A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598386



Internal ID6985522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160592814..160601738hg38UCSC Ensembl
Innerchr3:160592820..160601732hg38UCSC Ensembl
Outerchr3:160592808..160601744hg38UCSC Ensembl
chr3:160310602..160319526hg19UCSC Ensembl
Innerchr3:160310608..160319520hg19UCSC Ensembl
Outerchr3:160310596..160319532hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg388925
hg198925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11199680
SamplesNA12342
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598386
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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