A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11268665



Internal ID3929924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190176139..190178547hg38UCSC Ensembl
Innerchr3:190176144..190178542hg38UCSC Ensembl
Outerchr3:190176134..190178552hg38UCSC Ensembl
chr3:189893928..189896336hg19UCSC Ensembl
Innerchr3:189893933..189896331hg19UCSC Ensembl
Outerchr3:189893923..189896341hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382409
hg192409
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599066
Supporting Variants
SamplesHG03583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11268665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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