A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627004



Internal ID7013834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82749492..82752243hg38UCSC Ensembl
Innerchr11:82749514..82752222hg38UCSC Ensembl
Outerchr11:82749471..82752265hg38UCSC Ensembl
chr11:82460534..82463285hg19UCSC Ensembl
Innerchr11:82460556..82463264hg19UCSC Ensembl
Outerchr11:82460513..82463307hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14219118, essv14219119
SamplesNA18507, HG03172
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627004
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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