A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695651



Internal ID15432303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73022520..73029555hg38UCSC Ensembl
Innerchr13:73596658..73603693hg19UCSC Ensembl
Innerchr13:72494659..72501694hg18UCSC Ensembl
Innerchr13:72494659..72501694hg17UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg387036
hg197036
hg187036
hg177036
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517408
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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