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nsv906401

  • Variant Calls:15
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,287

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2021 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):32,550,536-32,556,822Question Mark
Overlapping variant regions from other studies: 2021 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):32,561,857-32,568,143Question Mark
Overlapping variant regions from other studies: 1361 SVs from 25 studies. See in: genome view    
Submitted genomic32,469,358-32,475,644Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv906401RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nsv906401RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nsv906401Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1515444copy number lossSP56197SNP arraySNP genotyping analysis19
nssv1519312copy number lossSP81009SNP arraySNP genotyping analysis15
nssv1519850copy number lossSP50580SNP arraySNP genotyping analysis13
nssv1520779copy number lossSP51243SNP arraySNP genotyping analysis5
nssv1524505copy number lossSP55064SNP arraySNP genotyping analysis11
nssv1525697copy number gainSP56773SNP arraySNP genotyping analysis10
nssv1527469copy number lossSP58443SNP arraySNP genotyping analysis9
nssv1527712copy number gainSP80945SNP arraySNP genotyping analysis5
nssv1534480copy number lossMS11632SNP arraySNP genotyping analysis18
nssv1539892copy number gainMS14562SNP arraySNP genotyping analysis7
nssv1541471copy number lossMS15317SNP arraySNP genotyping analysis9
nssv1545379copy number gainMS16752SNP arraySNP genotyping analysis7
nssv1549267copy number lossMS18159SNP arraySNP genotyping analysis15
nssv1557224copy number gainMS22499SNP arraySNP genotyping analysis11
nssv1563001copy number gainMS25813SNP arraySNP genotyping analysis8

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1515444RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1519312RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1519850RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1520779RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1524505RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1525697RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
dup
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1527469RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1527712RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
dup
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1534480RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1539892RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
dup
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1541471RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1545379RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
dup
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1549267RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
del
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1557224RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
dup
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1563001RemappedPerfectNC_000016.10:g.(32
550536_32551371)_(
32556599_32556822)
dup
GRCh38.p12First PassNC_000016.10Chr1632,550,53632,551,37132,556,59932,556,822
nssv1515444RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1519312RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1519850RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1520779RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1524505RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1525697RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
up
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1527469RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1527712RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
up
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1534480RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1539892RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
up
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1541471RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1545379RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
up
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1549267RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
el
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1557224RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
up
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1563001RemappedPerfectNC_000016.9:g.(325
61857_32562692)_(3
2567920_32568143)d
up
GRCh37.p13First PassNC_000016.9Chr1632,561,85732,562,69232,567,92032,568,143
nssv1515444Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1519312Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1519850Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1520779Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1524505Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1525697Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
up
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1527469Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1527712Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
up
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1534480Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1539892Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
up
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1541471Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1545379Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
up
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1549267Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
el
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1557224Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
up
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644
nssv1563001Submitted genomicNC_000016.8:g.(324
69358_32470193)_(3
2475421_32475644)d
up
NCBI36 (hg18)NC_000016.8Chr1632,469,35832,470,19332,475,42132,475,644

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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