A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585668



Internal ID16373077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19089508..19117621hg38UCSC Ensembl
Innerchr20:19070152..19098265hg19UCSC Ensembl
Innerchr20:19018152..19046265hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3828114
hg1928114
hg1828114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938598
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585668
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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