A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664894



Internal ID15054860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83163722..83168288hg38UCSC Ensembl
Innerchr16:83197327..83201893hg19UCSC Ensembl
Innerchr16:81754828..81759394hg18UCSC Ensembl
Innerchr16:81754828..81759394hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg384567
hg194567
hg184567
hg174567
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515825
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664894
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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