A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626792



Internal ID7013622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72141339..72179940hg38UCSC Ensembl
Innerchr11:72141489..72179790hg38UCSC Ensembl
Outerchr11:72141189..72180090hg38UCSC Ensembl
chr11:71852383..71890984hg19UCSC Ensembl
Innerchr11:71852533..71890834hg19UCSC Ensembl
Outerchr11:71852233..71891134hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3838602
hg1938602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208e214
Supporting Variantsessv14210770, essv14210773, essv14210772, essv14210769, essv14210771
SamplesHG00142, HG02634, NA19917, HG00266, HG03898
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626792
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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