A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585287



Internal ID16372696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3830786..3843810hg38UCSC Ensembl
Innerchr20:3811433..3824457hg19UCSC Ensembl
Innerchr20:3759433..3772457hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813025
hg1913025
hg1813025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937352
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585287
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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