A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376077



Internal ID22139800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90455192..90455270hg38UCSC Ensembl
chr14:90921536..90921614hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529508
Supporting Variants
SamplesHG00513
Known GenesLINC00642
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376077
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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