A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14313109



Internal ID22304366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43187628..43189111hg38UCSC Ensembl
chr4:43189645..43191128hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg381484
hg191484
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206322
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14313109
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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