A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684861



Internal ID15421513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105275596..105276911hg38UCSC Ensembl
Innerchr13:105927947..105929262hg19UCSC Ensembl
Innerchr13:104725948..104727263hg18UCSC Ensembl
Innerchr13:104725948..104727263hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg381316
hg191316
hg181316
hg171316
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520752
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684861
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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