A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14219484



Internal ID1934956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83140595..83149253hg38UCSC Ensembl
Innerchr11:83140595..83149253hg38UCSC Ensembl
Outerchr11:83140095..83149753hg38UCSC Ensembl
chr11:82851637..82860295hg19UCSC Ensembl
Innerchr11:82851637..82860295hg19UCSC Ensembl
Outerchr11:82851137..82860795hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388659
hg198659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627011
Supporting Variants
SamplesHG01802
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14219484
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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