A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625863



Internal ID7012697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32451027..32458111hg38UCSC Ensembl
Innerchr11:32451027..32458111hg38UCSC Ensembl
Outerchr11:32450527..32458611hg38UCSC Ensembl
chr11:32472573..32479657hg19UCSC Ensembl
Innerchr11:32472573..32479657hg19UCSC Ensembl
Outerchr11:32472073..32480157hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387085
hg197085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14084226, essv14084227
SamplesNA21122, HG03615
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625863
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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