A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213234



Internal ID22360242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:96308000..96323706hg38UCSC Ensembl
Outerchr9:99070282..99085988hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3815707
hg1915707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282861
SamplesHG00513
Known GenesSLC35D2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213234
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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