A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959878



Internal ID16253834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20346613..20438761hg38UCSC Ensembl
Innerchr3:20388105..20480253hg19UCSC Ensembl
Innerchr3:20363109..20455257hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3892149
hg1992149
hg1892149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589858
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)nssv959878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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