A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696488



Internal ID15086454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105467097..105473959hg38UCSC Ensembl
Innerchr13:106119446..106126308hg19UCSC Ensembl
Innerchr13:104917447..104924309hg18UCSC Ensembl
Innerchr13:104917447..104924309hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg386863
hg196863
hg186863
hg176863
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519018
Supporting Variants
Samples
Known GenesDAOA, DAOA-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696488
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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