A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598346



Internal ID6638612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158831759..159067480hg38UCSC Ensembl
chr3:158549548..158785269hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38235722
hg19235722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11198129, essv11198130
SamplesHG03919, NA20289
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598346
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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