A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004921



Internal ID22066552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:59732215..59738691hg38UCSC Ensembl
Outerchr8:59728360..59741517hg38UCSC Ensembl
Innerchr8:60644774..60651250hg19UCSC Ensembl
Outerchr8:60640919..60654076hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3813158
hg1913158
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154364
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004921
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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