A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213953



Internal ID22360741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3153051..3179182hg38UCSC Ensembl
Outerchr19:3153049..3179180hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3826132
hg1926132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14263378
SamplesHG00732
Known GenesGNA15, S1PR4
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213953
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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