A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225684



Internal ID22368744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42634598..42659652hg38UCSC Ensembl
Outerchr9:44311467..44336521hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3825055
hg1925055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14280333
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225684
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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