A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624822



Internal ID7011672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124932102..124937760hg38UCSC Ensembl
chr10:126620671..126626329hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385659
hg195659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963422, essv13963411, essv13963420, essv13963419, essv13963418, essv13963413, essv13963410, essv13963404, essv13963401, essv13963415, essv13963403, essv13963412, essv13963402, essv13963416, essv13963414, essv13963407, essv13963421, essv13963409, essv13963408, essv13963406, essv13963405, essv13963417
SamplesHG03300, HG02231, NA18486, HG03172, NA19098, NA19314, HG03095, NA19723, HG02582, HG03027, HG02537, NA19776, NA19654, HG01102, HG03301, HG02817, NA19320, NA19395, HG02896, HG01190, NA19712, NA19323
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624822
Frequency
Sample Size2504
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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