A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572794



Internal ID16360203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58638859..58642320hg38UCSC Ensembl
Innerchr16:58672763..58676224hg19UCSC Ensembl
Innerchr16:57230264..57233725hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383462
hg193462
hg183462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5159n54
Supporting Variantsnssv858710
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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