A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227432



Internal ID22369929
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282906
SamplesHG00731
Known GenesZNF169
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227432
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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