A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621199



Internal ID6661378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98044011..98052515hg38UCSC Ensembl
Innerchr9:98044511..98052015hg38UCSC Ensembl
Outerchr9:98043011..98053515hg38UCSC Ensembl
chr9:100806293..100814797hg19UCSC Ensembl
Innerchr9:100806793..100814297hg19UCSC Ensembl
Outerchr9:100805293..100815797hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg388505
hg198505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13574309, essv13574308, essv13574307, essv13574310
SamplesNA19378, HG03069, NA18510, NA19138
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621199
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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