A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14195772



Internal ID6743426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66536641..66537696hg38UCSC Ensembl
Innerchr11:66536641..66537696hg38UCSC Ensembl
Outerchr11:66536310..66538035hg38UCSC Ensembl
chr11:66304112..66305167hg19UCSC Ensembl
Innerchr11:66304112..66305167hg19UCSC Ensembl
Outerchr11:66303781..66305506hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626695
Supporting Variants
SamplesNA20862
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14195772
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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