A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695037



Internal ID15431689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41543792..41561964hg38UCSC Ensembl
Innerchr13:42117928..42136100hg19UCSC Ensembl
Innerchr13:41015928..41034100hg18UCSC Ensembl
Innerchr13:41015928..41034100hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3818173
hg1918173
hg1818173
hg1718173
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522257
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695037
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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