A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11165528



Internal ID6287016
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598013
Supporting Variants
SamplesNA19819
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11165528
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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