A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14282906



Internal ID22187765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:94261256..94277711hg38UCSC Ensembl
Outerchr9:97023538..97039993hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3816456
hg1916456
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227432
Supporting Variants
SamplesHG00731
Known GenesZNF169
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14282906
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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