A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999190



Internal ID19188224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:190093444..190120845hg38UCSC Ensembl
Outerchr4:191014599..191042000hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3827402
hg1927402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152007
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999190
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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