A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14212062



Internal ID6782606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73175020..73185975hg38UCSC Ensembl
Innerchr11:73175057..73185938hg38UCSC Ensembl
Outerchr11:73174983..73186012hg38UCSC Ensembl
chr11:72886065..72897020hg19UCSC Ensembl
Innerchr11:72886102..72896983hg19UCSC Ensembl
Outerchr11:72886028..72897057hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3810956
hg1910956
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626810
Supporting Variants
SamplesNA20882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14212062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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