A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370299



Internal ID22234169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63814886..63814947hg38UCSC Ensembl
chr14:64281604..64281665hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212496
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370299
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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