A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221698



Internal ID22365993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93698219..93719042hg38UCSC Ensembl
Outerchr9:96460501..96481324hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3820824
hg1920824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282810, nssv14282809
SamplesHG00512, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221698
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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