A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941595



Internal ID16235551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56779702..56787775hg38UCSC Ensembl
Innerchr20:55354758..55362831hg19UCSC Ensembl
Innerchr20:54788165..54796238hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg388074
hg198074
hg188074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586303
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)nssv941595
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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