A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571685



Internal ID16359094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23148799..23149484hg38UCSC Ensembl
Innerchr16:23160120..23160805hg19UCSC Ensembl
Innerchr16:23067621..23068306hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38686
hg19686
hg18686
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4955n54
Supporting Variantsnssv854157, nssv854155, nssv854161, nssv854154, nssv854159, nssv854158, nssv854156, nssv854160
Samples
Known GenesUSP31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571685
Frequency
Sample Size17421
Observed Gain3
Observed Loss5
Observed Complex0
Frequencyn/a


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