A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619843



Internal ID6660029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17478216..17483133hg38UCSC Ensembl
Innerchr9:17478230..17483119hg38UCSC Ensembl
Outerchr9:17478202..17483147hg38UCSC Ensembl
chr9:17478214..17483131hg19UCSC Ensembl
Innerchr9:17478228..17483117hg19UCSC Ensembl
Outerchr9:17478200..17483145hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg384918
hg194918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13412184
SamplesHG03259
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619843
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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