A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585724



Internal ID16026447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23661790..23741355hg38UCSC Ensembl
Innerchr20:23642427..23721992hg19UCSC Ensembl
Innerchr20:23590427..23669992hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3879566
hg1979566
hg1879566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152373
SamplesNINDS_73
Known GenesCST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585724
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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