A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859224



Internal ID15806494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76237670..76275183hg38UCSC Ensembl
Innerchr16:76271568..76309081hg19UCSC Ensembl
Innerchr16:74829069..74866582hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3837514
hg1937514
hg1837514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573017
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859224
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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