A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11025686



Internal ID6411115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60034997..60160949hg38UCSC Ensembl
chr3:60020723..60146677hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38125953
hg19125955
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596296
Supporting Variants
SamplesNA20357
Known GenesFHIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11025686
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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