A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999164



Internal ID19188709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149915347..149921248hg38UCSC Ensembl
Outerchr4:150836499..150842400hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg385902
hg195902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151979
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999164
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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