A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14050711



Internal ID6044563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22927609..23086160hg38UCSC Ensembl
chr11:22949155..23107706hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38158552
hg19158552
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625626
Supporting Variants
SamplesNA19445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14050711
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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