A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586578



Internal ID16027301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63558992..63570431hg38UCSC Ensembl
Innerchr20:62190345..62201784hg19UCSC Ensembl
Innerchr20:61660789..61672228hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811440
hg1911440
hg1811440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943756
Samples
Known GenesHELZ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586578
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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