A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595592



Internal ID6982910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24849977..24866642hg38UCSC Ensembl
Innerchr3:24849993..24866626hg38UCSC Ensembl
Outerchr3:24849961..24866658hg38UCSC Ensembl
chr3:24891468..24908133hg19UCSC Ensembl
Innerchr3:24891484..24908117hg19UCSC Ensembl
Outerchr3:24891452..24908149hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3816666
hg1916666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10950283, essv10950285, essv10950284
SamplesNA21137, HG03709, HG02697
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595592
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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