A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14372464



Internal ID22295361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20828565..20828633hg38UCSC Ensembl
chr14:21296724..21296792hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220422
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14372464
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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