A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572833



Internal ID16360242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60022184..60138126hg38UCSC Ensembl
Innerchr16:60056088..60172030hg19UCSC Ensembl
Innerchr16:58613589..58729531hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38115943
hg19115943
hg18115943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858907
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572833
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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