A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370385



Internal ID22193289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65780383..65782244hg38UCSC Ensembl
chr14:66247101..66248962hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381862
hg191862
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223702
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370385
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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