A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571688



Internal ID16359097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23149034..23158922hg38UCSC Ensembl
Innerchr16:23160355..23170243hg19UCSC Ensembl
Innerchr16:23067856..23077744hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg389889
hg199889
hg189889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv854165
Samples
Known GenesUSP31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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