A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11160825



Internal ID5992456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139284898..139286500hg38UCSC Ensembl
Innerchr3:139284900..139286499hg38UCSC Ensembl
Outerchr3:139284897..139286502hg38UCSC Ensembl
chr3:139003740..139005342hg19UCSC Ensembl
Innerchr3:139003742..139005341hg19UCSC Ensembl
Outerchr3:139003739..139005344hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381603
hg191603
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597936
Supporting Variants
SamplesNA19394
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11160825
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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