A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597114



Internal ID6984428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98406626..98412483hg38UCSC Ensembl
Innerchr3:98406629..98412480hg38UCSC Ensembl
Outerchr3:98406623..98412486hg38UCSC Ensembl
chr3:98125470..98131327hg19UCSC Ensembl
Innerchr3:98125473..98131324hg19UCSC Ensembl
Outerchr3:98125467..98131330hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg385858
hg195858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11074830, essv11074835, essv11074829, essv11074833, essv11074836, essv11074838, essv11074826, essv11074837, essv11074828, essv11074834, essv11074827, essv11074832, essv11074831, essv11074839
SamplesHG02890, HG02481, HG03130, NA18988, HG02105, HG02485, NA19307, HG03556, HG02573, NA18986, HG02009, HG01889, NA19257, HG01894
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597114
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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