A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609257



Internal ID6996179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63299250..63313323hg38UCSC Ensembl
chr6:64009155..64023228hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3814074
hg1914074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12389782, essv12389784, essv12389788, essv12389790, essv12389781, essv12389783, essv12389791, essv12389789, essv12389785, essv12389787, essv12389786
SamplesHG03593, HG04096, HG03717, HG03784, HG03861, HG03786, HG03771, HG03871, NA21095, HG03615, HG04056
Known GenesLGSN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609257
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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