A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14216357



Internal ID1672873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80860765..80864922hg38UCSC Ensembl
Innerchr11:80860768..80864919hg38UCSC Ensembl
Outerchr11:80860762..80864925hg38UCSC Ensembl
chr11:80571808..80575965hg19UCSC Ensembl
Innerchr11:80571811..80575962hg19UCSC Ensembl
Outerchr11:80571805..80575968hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384158
hg194158
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626939
Supporting Variants
SamplesHG01531
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14216357
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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