A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666612



Internal ID15403264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63858789..64359486hg38UCSC Ensembl
Innerchr13:64432922..64933618hg19UCSC Ensembl
Innerchr13:63330923..63831619hg18UCSC Ensembl
Innerchr13:63330923..63831619hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38500698
hg19500697
hg18500697
hg17500697
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516171
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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