A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625843



Internal ID7012677
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14079585, essv14079584, essv14079583, essv14079582
SamplesNA19917, HG03363, HG01447, NA20897
Known GenesDKFZp686K1684
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625843
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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