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nsv462159

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:269,179

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 582 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):50,664,839-50,934,017Question Mark
Overlapping variant regions from other studies: 582 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):49,960,673-50,229,851Question Mark
Overlapping variant regions from other studies: 57 SVs from 9 studies. See in: genome view    
Submitted genomic49,996,430-50,265,608Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv462159RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr550,664,83950,934,017
nsv462159RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr549,960,67350,229,851
nsv462159Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000005.8Chr549,996,43050,265,608

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv639384copy number gainSNP arraySNP genotyping analysis3

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv639384RemappedPerfectNC_000005.10:g.(?_
50664839)_(5093401
7_?)dup
GRCh38.p12First PassNC_000005.10Chr550,664,83950,934,017
nssv639384RemappedPerfectNC_000005.9:g.(?_4
9960673)_(50229851
_?)dup
GRCh37.p13First PassNC_000005.9Chr549,960,67350,229,851
nssv639384Submitted genomicNC_000005.8:g.(?_4
9996430)_(50265608
_?)dup
NCBI35 (hg17)NC_000005.8Chr549,996,43050,265,608

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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