U.S. flag

An official website of the United States government

nsv831920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:251,093

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 490 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):78,478,725-78,729,817Question Mark
Overlapping variant regions from other studies: 490 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):80,238,482-80,489,574Question Mark
Overlapping variant regions from other studies: 32 SVs from 3 studies. See in: genome view    
Submitted genomic79,908,488-80,159,580Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv831920RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1078,478,72578,729,817
nsv831920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1080,238,48280,489,574
nsv831920Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000010.8Chr1079,908,48880,159,580

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1448614copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1448614RemappedPerfectNC_000010.11:g.(78
478725_?)_(?_78729
817)del
GRCh38.p12First PassNC_000010.11Chr1078,478,72578,729,817
nssv1448614RemappedPerfectNC_000010.10:g.(80
238482_?)_(?_80489
574)del
GRCh37.p13First PassNC_000010.10Chr1080,238,48280,489,574
nssv1448614Submitted genomicNC_000010.8:g.(799
08488_?)_(?_801595
80)del
NCBI35 (hg17)NC_000010.8Chr1079,908,48880,159,580

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

Support Center