A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695498



Internal ID15085464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83525197..83531255hg38UCSC Ensembl
Innerchr16:83558802..83564860hg19UCSC Ensembl
Innerchr16:82116303..82122361hg18UCSC Ensembl
Innerchr16:82116303..82122361hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg386059
hg196059
hg186059
hg176059
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518084
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695498
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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