A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156833



Internal ID22087234
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv276n97
Supporting Variantsnssv4019983, nssv4019982
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156833
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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