A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281895



Internal ID22326274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:35979139..36004756hg38UCSC Ensembl
Outerchr9:35979136..36004753hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3825618
hg1925618
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214432
Supporting Variants
SamplesNA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281895
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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