A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625659



Internal ID7012493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23943347..23958070hg38UCSC Ensembl
Innerchr11:23943497..23957920hg38UCSC Ensembl
Outerchr11:23943197..23958220hg38UCSC Ensembl
chr11:23964893..23979616hg19UCSC Ensembl
Innerchr11:23965043..23979466hg19UCSC Ensembl
Outerchr11:23964743..23979766hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3814724
hg1914724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14058113
SamplesHG01790
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625659
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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