A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231199



Internal ID22372166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:131775352..131796747hg38UCSC Ensembl
Outerchr9:134650739..134672134hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253211
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231199
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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