A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019982



Internal ID22081613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8460307..8592908hg38UCSC Ensembl
Outerchr8:8459149..8593314hg38UCSC Ensembl
Innerchr8:8317817..8450418hg19UCSC Ensembl
Outerchr8:8316659..8450824hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38134166
hg19134166
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156833
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019982
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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