A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621204



Internal ID7008073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98083690..98086968hg38UCSC Ensembl
Innerchr9:98083840..98086818hg38UCSC Ensembl
Outerchr9:98083540..98087118hg38UCSC Ensembl
chr9:100845972..100849250hg19UCSC Ensembl
Innerchr9:100846122..100849100hg19UCSC Ensembl
Outerchr9:100845822..100849400hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383279
hg193279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13574316, essv13574319, essv13574315, essv13574318, essv13574317
SamplesHG00306, HG04038, HG01767, NA19712, HG03072
Known GenesTRIM14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621204
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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