A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515876



Internal ID8410151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42824708..43153107hg38UCSC Ensembl
Innerchr15:43116906..43445305hg19UCSC Ensembl
Innerchr15:40904198..41232597hg18UCSC Ensembl
Innerchr15:40904198..41232597hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38328400
hg19328400
hg18328400
hg17328400
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705714, nssv695338, nssv705373, nssv669551, nssv665118, nssv682487, nssv662075, nssv705701
Samples
Known GenesTMEM62, TTBK2, UBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515876
Frequency
Sample Size2026
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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