A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573435



Internal ID16014158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84425951..84582551hg38UCSC Ensembl
Innerchr16:84459557..84616157hg19UCSC Ensembl
Innerchr16:83017058..83173658hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38156601
hg19156601
hg18156601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5262n54
Supporting Variantsnssv862010
Samples
Known GenesATP2C2, COTL1, TLDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573435
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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