A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623008



Internal ID6663176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42424202..42526578hg38UCSC Ensembl
chr10:42919650..43022026hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38102377
hg19102377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13763858, essv13763857
SamplesHG03708, NA20804
Known GenesCCNYL2, LINC00839, ZNF37BP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623008
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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