A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005062



Internal ID22066693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139100475..139103770hg38UCSC Ensembl
Outerchr8:139098174..139105176hg38UCSC Ensembl
Innerchr8:140112718..140116013hg19UCSC Ensembl
Outerchr8:140110417..140117419hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg387003
hg197003
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154398
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005062
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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