A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610245



Internal ID6997162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104451435..104489873hg38UCSC Ensembl
chr6:104899310..104937748hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3838439
hg1938439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12495660, essv12495658, essv12495664, essv12495661, essv12495659, essv12495666, essv12495665, essv12495662, essv12495657, essv12495663
SamplesNA20798, HG04029, HG01524, NA20787, HG00436, HG01536, HG03755, HG02799, HG03920, HG01191
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610245
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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