A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571010



Internal ID16011733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:562698..661905hg38UCSC Ensembl
Innerchr16:612698..711905hg19UCSC Ensembl
Innerchr16:552699..651906hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3899208
hg1999208
hg1899208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4823n54
Supporting Variantsnssv851739
Samples
Known GenesC16orf11, C16orf13, FAM195A, NHLRC4, PIGQ, RAB40C, WDR90, WFIKKN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571010
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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