A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573465



Internal ID16014188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84721358..84756765hg38UCSC Ensembl
Innerchr16:84754964..84790371hg19UCSC Ensembl
Innerchr16:83312465..83347872hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3835408
hg1935408
hg1835408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862181
Samples
Known GenesUSP10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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