A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14232941



Internal ID570038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91089566..91175388hg38UCSC Ensembl
Innerchr11:91090066..91174888hg38UCSC Ensembl
Outerchr11:91088566..91176388hg38UCSC Ensembl
chr11:90822734..90908556hg19UCSC Ensembl
Innerchr11:90823234..90908056hg19UCSC Ensembl
Outerchr11:90821734..90909556hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3885823
hg1985823
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627236
Supporting Variants
SamplesHG00251
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14232941
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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