A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611652



Internal ID6998558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167194805..167242469hg38UCSC Ensembl
chr6:167608293..167655957hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3847665
hg1947665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643405, essv12643400, essv12643403, essv12643401, essv12643398, essv12643402, essv12643399, essv12643406, essv12643404
SamplesHG02890, HG03241, HG03518, HG02054, HG03460, HG02571, HG03428, NA20281, HG03401
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611652
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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