A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586303



Internal ID16373712
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941596, nssv941595, nssv941597
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586303
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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