A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14287282



Internal ID22219785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19523518..19523870hg38UCSC Ensembl
chr19:19634327..19634679hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219130
Supporting Variants
SamplesHG00733
Known GenesNDUFA13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14287282
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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