A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621433



Internal ID7008302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109356638..109361875hg38UCSC Ensembl
Innerchr9:109356639..109361874hg38UCSC Ensembl
Outerchr9:109356637..109361876hg38UCSC Ensembl
chr9:112118918..112124155hg19UCSC Ensembl
Innerchr9:112118919..112124154hg19UCSC Ensembl
Outerchr9:112118917..112124156hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385238
hg195238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13595910, essv13595909, essv13595908, essv13595911, essv13595907
SamplesNA18574, HG00982, NA19434, HG00513, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621433
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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