A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702377



Internal ID15439029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66803291..66804320hg38UCSC Ensembl
Innerchr15:67095629..67096658hg19UCSC Ensembl
Innerchr15:64882683..64883712hg18UCSC Ensembl
Innerchr15:64882683..64883712hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381030
hg191030
hg181030
hg171030
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520187
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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