A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665118



Internal ID15055084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42851800..43153107hg38UCSC Ensembl
Innerchr15:43143998..43445305hg19UCSC Ensembl
Innerchr15:40931290..41232597hg18UCSC Ensembl
Innerchr15:40931290..41232597hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38301308
hg19301308
hg18301308
hg17301308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515876
Supporting Variants
Samples
Known GenesTMEM62, TTBK2, UBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665118
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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