A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065912



Internal ID18808443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83220154..83381450hg38UCSC Ensembl
Innerchr16:83253759..83415055hg19UCSC Ensembl
Innerchr16:81811260..81972556hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38161297
hg19161297
hg18161297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559930
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)nsv1065912
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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