A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862003



Internal ID15809273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84298994..84575953hg38UCSC Ensembl
Innerchr16:84332600..84609559hg19UCSC Ensembl
Innerchr16:82890101..83167060hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38276960
hg19276960
hg18276960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573425
Supporting Variants
Samples
Known GenesATP2C2, COTL1, TLDC1, WFDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv862003
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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