A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573123



Internal ID16360532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77096442..77126729hg38UCSC Ensembl
Innerchr16:77130339..77160626hg19UCSC Ensembl
Innerchr16:75687840..75718127hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3830288
hg1930288
hg1830288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5215n54
Supporting Variantsnssv860786
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573123
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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