A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14191237



Internal ID3810975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65757841..65763470hg38UCSC Ensembl
Innerchr11:65757853..65763459hg38UCSC Ensembl
Outerchr11:65757830..65763482hg38UCSC Ensembl
chr11:65525312..65530941hg19UCSC Ensembl
Innerchr11:65525324..65530930hg19UCSC Ensembl
Outerchr11:65525301..65530953hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385630
hg195630
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626679
Supporting Variants
SamplesHG03452
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14191237
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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