A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586305



Internal ID16373714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56829503..56851763hg38UCSC Ensembl
Innerchr20:55404559..55426819hg19UCSC Ensembl
Innerchr20:54837966..54860226hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3822261
hg1922261
hg1822261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7617n54
Supporting Variantsnssv941599
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586305
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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