A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619856



Internal ID7006730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17809991..17828854hg38UCSC Ensembl
Innerchr9:17809991..17828854hg38UCSC Ensembl
Outerchr9:17809733..17829100hg38UCSC Ensembl
chr9:17809989..17828852hg19UCSC Ensembl
Innerchr9:17809989..17828852hg19UCSC Ensembl
Outerchr9:17809731..17829098hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3818864
hg1918864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13412265
SamplesNA18564
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619856
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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