A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572357



Internal ID16359766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34939284..34957624hg38UCSC Ensembl
Innerchr16:34173678..34191995hg19UCSC Ensembl
Innerchr16:34031179..34049496hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3818341
hg1918318
hg1818318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv856198
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572357
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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