A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697917



Internal ID15087883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82739263..82742784hg38UCSC Ensembl
Innerchr16:82772868..82776389hg19UCSC Ensembl
Innerchr16:81330369..81333890hg18UCSC Ensembl
Innerchr16:81330369..81333890hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg383522
hg193522
hg183522
hg173522
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521310
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697917
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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