A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14282799



Internal ID22199897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67805475..67819020hg38UCSC Ensembl
Outerchr9:46018489..46034792hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813546
hg1916304
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212260
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14282799
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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