A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645433



Internal ID7032183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18197350..18198517hg38UCSC Ensembl
Innerchr20:18197350..18198517hg38UCSC Ensembl
Outerchr20:18197060..18198843hg38UCSC Ensembl
chr20:18177994..18179161hg19UCSC Ensembl
Innerchr20:18177994..18179161hg19UCSC Ensembl
Outerchr20:18177704..18179487hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381168
hg191168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16154798, essv16154812, essv16154804, essv16154795, essv16154801, essv16154811, essv16154802, essv16154796, essv16154806, essv16154793, essv16154794, essv16154805, essv16154797, essv16154809, essv16154799, essv16154803, essv16154800, essv16154808, essv16154810, essv16154807
SamplesNA11920, HG02231, HG00318, HG01682, HG01510, HG00253, NA20524, HG00332, HG01684, HG03781, HG01791, HG00157, HG01679, HG00382, HG01272, NA12046, HG00107, HG00186, HG00131, NA12154
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645433
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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