A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11199680



Internal ID4872910
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598386
Supporting Variants
SamplesNA12342
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11199680
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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