A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14315372



Internal ID22126405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98679989..98684544hg38UCSC Ensembl
chr4:99601140..99605695hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg384556
hg194556
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207453
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14315372
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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