A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14095012



Internal ID6121609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37742851..37820265hg38UCSC Ensembl
chr11:37764401..37841815hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3877415
hg1977415
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625989
Supporting Variants
SamplesNA19657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14095012
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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