A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597923



Internal ID6985061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138789951..138794660hg38UCSC Ensembl
chr3:138508793..138513502hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384710
hg194710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv941e214
Supporting Variantsessv11160790, essv11160791
SamplesHG00179, HG01926
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597923
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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