A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597113



Internal ID6984427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98392750..98405058hg38UCSC Ensembl
Innerchr3:98392751..98405058hg38UCSC Ensembl
Outerchr3:98392750..98405059hg38UCSC Ensembl
chr3:98111594..98123902hg19UCSC Ensembl
Innerchr3:98111595..98123902hg19UCSC Ensembl
Outerchr3:98111594..98123903hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3812309
hg1912309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11074817, essv11074820, essv11074825, essv11074816, essv11074818, essv11074822, essv11074813, essv11074821, essv11074815, essv11074824, essv11074819, essv11074814, essv11074823
SamplesHG03479, HG01067, HG02885, HG01092, HG01047, HG03397, HG02982, HG03473, HG02464, HG02814, HG03049, NA19474, NA19146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597113
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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