A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14210777



Internal ID430513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72263735..72264607hg38UCSC Ensembl
Innerchr11:72263735..72264607hg38UCSC Ensembl
Outerchr11:72263530..72264828hg38UCSC Ensembl
chr11:71974779..71975651hg19UCSC Ensembl
Innerchr11:71974779..71975651hg19UCSC Ensembl
Outerchr11:71974574..71975872hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626795
Supporting Variants
SamplesHG00131
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14210777
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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