A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14263589



Internal ID22276311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15910331..15943538hg38UCSC Ensembl
Outerchr19:16021141..16054348hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3833208
hg1933208
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214680
Supporting Variants
SamplesNA19239
Known GenesCYP4F11
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14263589
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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