A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598882



Internal ID6639147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181001910..181010235hg38UCSC Ensembl
Innerchr3:181001917..181010228hg38UCSC Ensembl
Outerchr3:181001903..181010242hg38UCSC Ensembl
chr3:180719698..180728023hg19UCSC Ensembl
Innerchr3:180719705..180728016hg19UCSC Ensembl
Outerchr3:180719691..180728030hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg388326
hg198326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv958e214
Supporting Variantsessv11251120, essv11251121
SamplesHG02323, HG03354
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598882
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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