A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626571



Internal ID7013403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61041380..61046528hg38UCSC Ensembl
Innerchr11:61041380..61046528hg38UCSC Ensembl
Outerchr11:61041061..61046846hg38UCSC Ensembl
chr11:60808852..60814000hg19UCSC Ensembl
Innerchr11:60808852..60814000hg19UCSC Ensembl
Outerchr11:60808533..60814318hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385149
hg195149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14176261, essv14176262, essv14176260
SamplesHG02250, HG00419, HG00463
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626571
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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