A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628039



Internal ID7014864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128054398..128065562hg38UCSC Ensembl
Innerchr11:128054436..128065524hg38UCSC Ensembl
Outerchr11:128054360..128065600hg38UCSC Ensembl
chr11:127924293..127935457hg19UCSC Ensembl
Innerchr11:127924331..127935419hg19UCSC Ensembl
Outerchr11:127924255..127935495hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811165
hg1911165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14306851
SamplesHG00607
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628039
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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