A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621153



Internal ID7008022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95375855..95383059hg38UCSC Ensembl
Innerchr9:95375893..95383021hg38UCSC Ensembl
Outerchr9:95375817..95383097hg38UCSC Ensembl
chr9:98138137..98145341hg19UCSC Ensembl
Innerchr9:98138175..98145303hg19UCSC Ensembl
Outerchr9:98138099..98145379hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387205
hg197205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13571960
SamplesNA19323
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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