A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317692



Internal ID4319511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132696494..132705453hg38UCSC Ensembl
Innerchr11:132696550..132705397hg38UCSC Ensembl
Outerchr11:132696438..132705509hg38UCSC Ensembl
chr11:132566389..132575348hg19UCSC Ensembl
Innerchr11:132566445..132575292hg19UCSC Ensembl
Outerchr11:132566333..132575404hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg388960
hg198960
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628128
Supporting Variants
SamplesHG01204
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317692
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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