A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004847



Internal ID22066478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40326278..40331992hg38UCSC Ensembl
Outerchr8:40324598..40335391hg38UCSC Ensembl
Innerchr8:40183797..40189511hg19UCSC Ensembl
Outerchr8:40182117..40192910hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810794
hg1910794
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154346
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004847
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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