A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281950



Internal ID22270913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107664212..107690784hg38UCSC Ensembl
Outerchr9:110426493..110453065hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3826573
hg1926573
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217920
Supporting Variants
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281950
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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