A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585721



Internal ID16026444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23254062..23312212hg38UCSC Ensembl
Innerchr20:23234699..23292849hg19UCSC Ensembl
Innerchr20:23182699..23240849hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3858151
hg1958151
hg1858151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152371
SamplesHGDP01157
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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