A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14076658



Internal ID4908043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29381180..29396838hg38UCSC Ensembl
Innerchr11:29381180..29396838hg38UCSC Ensembl
Outerchr11:29380680..29397338hg38UCSC Ensembl
chr11:29402727..29418385hg19UCSC Ensembl
Innerchr11:29402727..29418385hg19UCSC Ensembl
Outerchr11:29402227..29418885hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3815659
hg1915659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625796
Supporting Variants
SamplesNA12748
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14076658
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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