A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698347



Internal ID15434999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66801293..66804320hg38UCSC Ensembl
Innerchr15:67093631..67096658hg19UCSC Ensembl
Innerchr15:64880685..64883712hg18UCSC Ensembl
Innerchr15:64880685..64883712hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383028
hg193028
hg183028
hg173028
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522717
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698347
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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