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nsv879357

  • Variant Calls:23
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50,426

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1561 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):68,581,133-68,631,558Question Mark
Overlapping variant regions from other studies: 1561 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):69,446,851-69,497,276Question Mark
Overlapping variant regions from other studies: 949 SVs from 35 studies. See in: genome view    
Submitted genomic69,129,446-69,179,871Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv879357RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nsv879357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nsv879357Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr469,129,44669,131,95869,163,18869,179,871

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1552622copy number gainMS19553SNP arraySNP genotyping analysis10
nssv1564755copy number gainIS30294SNP arraySNP genotyping analysis15
nssv1570910copy number gainIS32329SNP arraySNP genotyping analysis11
nssv1572505copy number gainIS33087SNP arraySNP genotyping analysis13
nssv1575478copy number gainIS33749SNP arraySNP genotyping analysis8
nssv1576065copy number gainIS33865SNP arraySNP genotyping analysis11
nssv1582272copy number gainIS35895SNP arraySNP genotyping analysis13
nssv1584075copy number gainIS36798SNP arraySNP genotyping analysis10
nssv1584533copy number gainIS37062SNP arraySNP genotyping analysis9
nssv1586551copy number gainIS37860SNP arraySNP genotyping analysis15
nssv1588089copy number gainIS38152SNP arraySNP genotyping analysis10
nssv1588428copy number lossIS38198SNP arraySNP genotyping analysis13
nssv1588992copy number gainIS38274SNP arraySNP genotyping analysis11
nssv1591183copy number gainIS38649SNP arraySNP genotyping analysis9
nssv1591535copy number gainIS38972SNP arraySNP genotyping analysis14
nssv1593709copy number gainIS39499SNP arraySNP genotyping analysis5
nssv1595250copy number gainIS40192SNP arraySNP genotyping analysis11
nssv1595523copy number gainIS40245SNP arraySNP genotyping analysis10
nssv1596795copy number gainIS40643SNP arraySNP genotyping analysis15
nssv1597651copy number gainIS40956SNP arraySNP genotyping analysis16
nssv1597894copy number gainIS40802SNP arraySNP genotyping analysis9
nssv1598042copy number gainIS40874SNP arraySNP genotyping analysis14
nssv1599246copy number gainIS41497SNP arraySNP genotyping analysis12

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1552622RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1564755RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1570910RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1572505RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1575478RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1576065RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1582272RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1584075RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1584533RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1586551RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1588089RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1588428RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
del
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1588992RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1591183RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1591535RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1593709RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1595250RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1595523RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1596795RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1597651RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1597894RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1598042RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1599246RemappedPerfectNC_000004.12:g.(68
581133_68583645)_(
68614875_68631558)
dup
GRCh38.p12First PassNC_000004.12Chr468,581,13368,583,64568,614,87568,631,558
nssv1552622RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1564755RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1570910RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1572505RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1575478RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1576065RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1582272RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1584075RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1584533RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1586551RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1588089RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1588428RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
del
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1588992RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1591183RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1591535RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1593709RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1595250RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1595523RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1596795RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1597651RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1597894RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1598042RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1599246RemappedPerfectNC_000004.11:g.(69
446851_69449363)_(
69480593_69497276)
dup
GRCh37.p13First PassNC_000004.11Chr469,446,85169,449,36369,480,59369,497,276
nssv1552622Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1564755Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1570910Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1572505Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1575478Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1576065Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1582272Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1584075Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1584533Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1586551Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1588089Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1588428Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
del
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1588992Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1591183Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1591535Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1593709Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1595250Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1595523Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1596795Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1597651Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1597894Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1598042Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871
nssv1599246Submitted genomicNC_000004.10:g.(69
129446_69131958)_(
69163188_69179871)
dup
NCBI36 (hg18)NC_000004.10Chr469,129,44669,131,95869,163,18869,179,871

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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