A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626827



Internal ID6666975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73981882..73989713hg38UCSC Ensembl
Innerchr11:73982382..73989213hg38UCSC Ensembl
Outerchr11:73980882..73990713hg38UCSC Ensembl
chr11:73692927..73700758hg19UCSC Ensembl
Innerchr11:73693427..73700258hg19UCSC Ensembl
Outerchr11:73691927..73701758hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg387832
hg197832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14212733, essv14212732
SamplesHG00867, HG01813
Known GenesUCP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626827
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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