A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14282859



Internal ID22156140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93730936..93752120hg38UCSC Ensembl
Outerchr9:96493218..96514402hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3821185
hg1921185
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222395
Supporting Variants
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14282859
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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