A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586520



Internal ID16373929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62673928..62693306hg38UCSC Ensembl
Innerchr20:61305280..61324658hg19UCSC Ensembl
Innerchr20:60775725..60795103hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3819379
hg1919379
hg1819379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942275
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586520
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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