A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14306851



Internal ID976667
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628039
Supporting Variants
SamplesHG00607
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14306851
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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