A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999251



Internal ID19192330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:91870071..91874472hg38UCSC Ensembl
Outerchr8:92882299..92886700hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg384402
hg194402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152068
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999251
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer