A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236623



Internal ID22373639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38732506..38734837hg38UCSC Ensembl
Outerchr9:38732503..38734834hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253224
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236623
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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