A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585431



Internal ID16372840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12598696..12627423hg38UCSC Ensembl
Innerchr20:12579343..12608070hg19UCSC Ensembl
Innerchr20:12527343..12556070hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3828728
hg1928728
hg1828728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151204
Samples1780862459_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585431
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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