A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996722



Internal ID19186819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:3570272..3610373hg38UCSC Ensembl
Outerchr4:3571999..3612100hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3840102
hg1940102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152115
Supporting Variants
SamplesKWB1
Known GenesLINC00955
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996722
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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