U.S. flag

An official website of the United States government

nsv830436

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:211,484

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 597 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):105,856,569-106,068,052Question Mark
Overlapping variant regions from other studies: 597 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):105,192,270-105,403,753Question Mark
Overlapping variant regions from other studies: 44 SVs from 5 studies. See in: genome view    
Submitted genomic105,220,169-105,431,652Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv830436RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5105,856,569106,068,052
nsv830436RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5105,192,270105,403,753
nsv830436Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000005.8Chr5105,220,169105,431,652

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1444956copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1444956RemappedPerfectNC_000005.10:g.(10
5856569_?)_(?_1060
68052)del
GRCh38.p12First PassNC_000005.10Chr5105,856,569106,068,052
nssv1444956RemappedPerfectNC_000005.9:g.(105
192270_?)_(?_10540
3753)del
GRCh37.p13First PassNC_000005.9Chr5105,192,270105,403,753
nssv1444956Submitted genomicNC_000005.8:g.(105
220169_?)_(?_10543
1652)del
NCBI35 (hg17)NC_000005.8Chr5105,220,169105,431,652

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