A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607326



Internal ID6994260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158217374..158228332hg38UCSC Ensembl
Innerchr5:158217424..158227897hg38UCSC Ensembl
Outerchr5:158217324..158228382hg38UCSC Ensembl
chr5:157644382..157655340hg19UCSC Ensembl
Innerchr5:157644432..157654905hg19UCSC Ensembl
Outerchr5:157644332..157655390hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3810959
hg1910959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12111663, essv12111662, essv12111660, essv12111659, essv12111661
SamplesHG01177, HG01048, HG01107, HG01205, HG01089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607326
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer