A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602939



Internal ID6989972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:162505484..162621258hg38UCSC Ensembl
chr4:163426636..163542410hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38115775
hg19115775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11674184
SamplesNA21102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602939
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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