A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997216



Internal ID19189007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:19097607..19103008hg38UCSC Ensembl
Outerchr3:19139099..19144500hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385402
hg195402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145851
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997216
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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