A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700536



Internal ID15090502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83607901..83607971hg38UCSC Ensembl
Innerchr16:83641506..83641576hg19UCSC Ensembl
Innerchr16:82199007..82199077hg18UCSC Ensembl
Innerchr16:82199007..82199077hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3871
hg1971
hg1871
hg1771
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524580
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700536
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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