A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3243886



Internal ID22375702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:105265765..105308697hg38UCSC Ensembl
Outerchr9:108028046..108070978hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281395
SamplesNA19239
Known GenesSLC44A1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3243886
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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