A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586579



Internal ID16373988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63571331..63571969hg38UCSC Ensembl
Innerchr20:62202684..62203322hg19UCSC Ensembl
Innerchr20:61673128..61673766hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38639
hg19639
hg18639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7669n54
Supporting Variantsnssv943757
Samples
Known GenesHELZ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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