A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213009



Internal ID22360091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:87912561..87935800hg38UCSC Ensembl
Outerchr9:90527476..90550715hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3823240
hg1923240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282871, nssv14282872
SamplesHG00732, HG00514
Known GenesSPATA31C1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213009
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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