nsv829765

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:150,234

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 194 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):156,850,474-157,000,707Question Mark
Overlapping variant regions from other studies: 194 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):156,568,263-156,718,496Question Mark
Overlapping variant regions from other studies: 10 SVs from 2 studies. See in: genome view    
Submitted genomic158,050,965-158,201,198Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv829765RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000003.12Chr3156,850,474157,000,707
nsv829765RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000003.11Chr3156,568,263156,718,496
nsv829765Submitted genomicNCBI35 (hg17)NC_000003.9Chr3158,050,965158,201,198

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1443131copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nssv1443131RemappedPerfectNC_000003.12:g.(15
6850474_?)_(?_1570
00707)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000003.12Chr3156,850,474157,000,707
nssv1443131RemappedPerfectNC_000003.11:g.(15
6568263_?)_(?_1567
18496)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000003.11Chr3156,568,263156,718,496
nssv1443131Submitted genomicNC_000003.9:g.(158
050965_?)_(?_15820
1198)del
NCBI35 (hg17)NC_000003.9Chr3158,050,965158,201,198

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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