A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572792



Internal ID16360201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58634662..58642375hg38UCSC Ensembl
Innerchr16:58668566..58676279hg19UCSC Ensembl
Innerchr16:57226067..57233780hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387714
hg197714
hg187714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5158n54
Supporting Variantsnssv858708
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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