A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14174280



Internal ID6867980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58908765..58913607hg38UCSC Ensembl
Innerchr11:58908799..58913573hg38UCSC Ensembl
Outerchr11:58908731..58913641hg38UCSC Ensembl
chr11:58676238..58681080hg19UCSC Ensembl
Innerchr11:58676272..58681046hg19UCSC Ensembl
Outerchr11:58676204..58681114hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg384843
hg194843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626527
Supporting Variants
SamplesNA21094
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14174280
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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