A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571682



Internal ID16359091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23148695..23149406hg38UCSC Ensembl
Innerchr16:23160016..23160727hg19UCSC Ensembl
Innerchr16:23067517..23068228hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38712
hg19712
hg18712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4956n54
Supporting Variantsnssv854147
Samples
Known GenesUSP31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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