A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004364



Internal ID22065995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32825580..32830895hg38UCSC Ensembl
Outerchr8:32821348..32834588hg38UCSC Ensembl
Innerchr8:32683098..32688413hg19UCSC Ensembl
Outerchr8:32678866..32692106hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3813241
hg1913241
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154335
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004364
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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