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nsv940692

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,774

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 78 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):229,066-237,839Question Mark
Overlapping variant regions from other studies: 78 SVs from 9 studies. See in: genome view    
Submitted genomic95,733-104,506Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv940692RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY229,066229,066237,839237,839
nsv940692Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000024.9ChrY95,73395,733104,506104,506

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv1671721copy number gain1Oligo aCGHProbe signal intensity31,040

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1671721RemappedPerfectNC_000024.10:g.(22
9066_?)_(?_237839)
dup
GRCh38.p12First PassNC_000024.10ChrY229,066237,839
nssv1671721Submitted genomicNC_000024.9:g.(957
33_?)_(?_104506)du
p
GRCh37 (hg19)NC_000024.9ChrY95,733104,506

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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