A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14373629



Internal ID22155638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86287071..86287135hg38UCSC Ensembl
chr14:86753415..86753479hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222014
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14373629
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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