A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573434



Internal ID16014157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84425951..84455427hg38UCSC Ensembl
Innerchr16:84459557..84489033hg19UCSC Ensembl
Innerchr16:83017058..83046534hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3829477
hg1929477
hg1829477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862009
Samples
Known GenesATP2C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573434
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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