A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610802



Internal ID6997719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131076793..131085252hg38UCSC Ensembl
chr6:131397933..131406392hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg388460
hg198460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12551016, essv12551015
SamplesNA11894, HG01776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610802
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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