A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573396



Internal ID16014119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83409465..83458397hg38UCSC Ensembl
Innerchr16:83443070..83492002hg19UCSC Ensembl
Innerchr16:82000571..82049503hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3848933
hg1948933
hg1848933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861983
Samples
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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