A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596340



Internal ID6983657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61383158..61432945hg38UCSC Ensembl
chr3:61368832..61418619hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3849788
hg1949788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11026102
SamplesHG03673
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596340
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