A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621197



Internal ID7008066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98019177..98019488hg38UCSC Ensembl
Innerchr9:98019178..98019488hg38UCSC Ensembl
Outerchr9:98019177..98019489hg38UCSC Ensembl
chr9:100781459..100781770hg19UCSC Ensembl
Innerchr9:100781460..100781770hg19UCSC Ensembl
Outerchr9:100781459..100781771hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13574287, essv13574288
SamplesHG01768, HG02304
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621197
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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