A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663239



Internal ID15399891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60977248..60986023hg38UCSC Ensembl
Innerchr15:61269447..61278222hg19UCSC Ensembl
Innerchr15:59056739..59065514hg18UCSC Ensembl
Innerchr15:59056739..59065514hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg388776
hg198776
hg188776
hg178776
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520362
Supporting Variants
Samples
Known GenesRORA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663239
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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