A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11163684



Internal ID2570883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141041495..141046353hg38UCSC Ensembl
Innerchr3:141041497..141046352hg38UCSC Ensembl
Outerchr3:141041494..141046355hg38UCSC Ensembl
chr3:140760337..140765195hg19UCSC Ensembl
Innerchr3:140760339..140765194hg19UCSC Ensembl
Outerchr3:140760336..140765197hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg384859
hg194859
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597968
Supporting Variants
SamplesHG02281
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11163684
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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