A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223702



Internal ID22367392
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370383, nssv14370388, nssv14370387, nssv14370386, nssv14370389, nssv14370385, nssv14370384, nssv14370390, nssv14370382
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223702
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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