A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622232



Internal ID7009091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5609236..5660606hg38UCSC Ensembl
chr10:5651199..5702569hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851371
hg1951371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13685657, essv13685659, essv13685656, essv13685654, essv13685655, essv13685653, essv13685652, essv13685658
SamplesNA20359, NA19131, NA19200, NA20362, HG03473, NA19143, HG03157, HG03271
Known GenesASB13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622232
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer