A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004972



Internal ID22066603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85200494..85202500hg38UCSC Ensembl
Outerchr8:85196395..85208660hg38UCSC Ensembl
Innerchr8:86112729..86114735hg19UCSC Ensembl
Outerchr8:86108630..86120895hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3812266
hg1912266
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154371
Supporting Variants
Samples
Known GenesE2F5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004972
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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