A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063276



Internal ID18805807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83528261..83583989hg38UCSC Ensembl
Innerchr16:83561866..83617594hg19UCSC Ensembl
Innerchr16:82119367..82175095hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3855729
hg1955729
hg1855729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559936
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063276
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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