A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700149



Internal ID15436801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112858017..112885580hg38UCSC Ensembl
Innerchr13:113512331..113539894hg19UCSC Ensembl
Innerchr13:112560332..112587895hg18UCSC Ensembl
Innerchr13:112560332..112587895hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3827564
hg1927564
hg1827564
hg1727564
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524253
Supporting Variants
Samples
Known GenesATP11A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700149
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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