A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598013



Internal ID6985149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142923010..142924608hg38UCSC Ensembl
Innerchr3:142923018..142924600hg38UCSC Ensembl
Outerchr3:142923002..142924616hg38UCSC Ensembl
chr3:142641852..142643450hg19UCSC Ensembl
Innerchr3:142641860..142643442hg19UCSC Ensembl
Outerchr3:142641844..142643458hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381599
hg191599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11165527, essv11165528
SamplesNA19819, HG01405
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598013
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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