A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596021



Internal ID6983339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43663965..43677052hg38UCSC Ensembl
chr3:43705457..43718544hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3813088
hg1913088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10993171, essv10993169, essv10993170
SamplesNA20910, NA12889, HG00380
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596021
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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