A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645681



Internal ID7032430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33458554..33460260hg38UCSC Ensembl
Innerchr20:33458554..33460260hg38UCSC Ensembl
Outerchr20:33458354..33460490hg38UCSC Ensembl
chr20:32046360..32048066hg19UCSC Ensembl
Innerchr20:32046360..32048066hg19UCSC Ensembl
Outerchr20:32046160..32048296hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381707
hg191707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16175359, essv16175358
SamplesNA19314, NA19462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645681
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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