A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623024



Internal ID7009881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42689080..42751910hg38UCSC Ensembl
chr10:43184528..43247358hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3862831
hg1962831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764085, essv13764083, essv13764084
SamplesNA20532, NA20589, HG02236
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623024
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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