A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699107



Internal ID15089073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41144691..41186811hg38UCSC Ensembl
Innerchr13:41718827..41760947hg19UCSC Ensembl
Innerchr13:40616827..40658947hg18UCSC Ensembl
Innerchr13:40616827..40658947hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3842121
hg1942121
hg1842121
hg1742121
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523358
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699107
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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