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nsv879257

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:162,545

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2081 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):68,499,144-68,661,688Question Mark
Overlapping variant regions from other studies: 2081 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):69,364,862-69,527,406Question Mark
Overlapping variant regions from other studies: 1126 SVs from 35 studies. See in: genome view    
Submitted genomic69,047,457-69,210,001Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv879257RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nsv879257RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nsv879257Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr469,047,45769,064,67569,195,50069,210,001

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1531561copy number gainMS10545SNP arraySNP genotyping analysis9
nssv1535149copy number gainMS12041SNP arraySNP genotyping analysis8
nssv1536697copy number gainMS12913SNP arraySNP genotyping analysis10
nssv1540398copy number gainMS14828SNP arraySNP genotyping analysis9
nssv1542193copy number gainMS15704SNP arraySNP genotyping analysis32
nssv1543895copy number gainMS16153SNP arraySNP genotyping analysis569
nssv1544121copy number gainMS16265SNP arraySNP genotyping analysis7
nssv1547407copy number gainMS17371SNP arraySNP genotyping analysis12
nssv1551630copy number gainMS18956SNP arraySNP genotyping analysis15
nssv1552215copy number gainMS19289SNP arraySNP genotyping analysis8
nssv1552914copy number gainMS19638SNP arraySNP genotyping analysis16
nssv1567809copy number gainIS31147SNP arraySNP genotyping analysis12
nssv1575362copy number gainIS33721SNP arraySNP genotyping analysis12
nssv1578629copy number gainIS34821SNP arraySNP genotyping analysis8
nssv1584751copy number gainIS37167SNP arraySNP genotyping analysis8
nssv1598317copy number gainIS40849SNP arraySNP genotyping analysis12

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1531561RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1535149RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1536697RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1540398RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1542193RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1543895RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1544121RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1547407RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1551630RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1552215RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1552914RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1567809RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1575362RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1578629RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1584751RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1598317RemappedPerfectNC_000004.12:g.(68
499144_68516362)_(
68647187_68661688)
dup
GRCh38.p12First PassNC_000004.12Chr468,499,14468,516,36268,647,18768,661,688
nssv1531561RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1535149RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1536697RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1540398RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1542193RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1543895RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1544121RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1547407RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1551630RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1552215RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1552914RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1567809RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1575362RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1578629RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1584751RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1598317RemappedPerfectNC_000004.11:g.(69
364862_69382080)_(
69512905_69527406)
dup
GRCh37.p13First PassNC_000004.11Chr469,364,86269,382,08069,512,90569,527,406
nssv1531561Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1535149Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1536697Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1540398Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1542193Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1543895Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1544121Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1547407Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1551630Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1552215Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1552914Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1567809Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1575362Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1578629Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1584751Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001
nssv1598317Submitted genomicNC_000004.10:g.(69
047457_69064675)_(
69195500_69210001)
dup
NCBI36 (hg18)NC_000004.10Chr469,047,45769,064,67569,195,50069,210,001

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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