A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14079583



Internal ID3727644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31850228..31878565hg38UCSC Ensembl
Innerchr11:31850378..31878415hg38UCSC Ensembl
Outerchr11:31850078..31878715hg38UCSC Ensembl
chr11:31871774..31900111hg19UCSC Ensembl
Innerchr11:31871924..31899961hg19UCSC Ensembl
Outerchr11:31871624..31900261hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3828338
hg1928338
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625843
Supporting Variants
SamplesHG03363
Known GenesDKFZp686K1684
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14079583
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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