A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390818



Internal ID22197062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94343049..94346447hg38UCSC Ensembl
chr14:94809386..94812784hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383399
hg193399
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215412
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390818
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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