A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14179726



Internal ID3495844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62679843..62680601hg38UCSC Ensembl
Innerchr11:62679893..62680551hg38UCSC Ensembl
Outerchr11:62679763..62680681hg38UCSC Ensembl
chr11:62447315..62448073hg19UCSC Ensembl
Innerchr11:62447365..62448023hg19UCSC Ensembl
Outerchr11:62447235..62448153hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626612
Supporting Variants
SamplesHG03105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14179726
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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