A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3240659



Internal ID22374759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:66778497..66794091hg38UCSC Ensembl
Outerchr9:40898783..40914372hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3811427
hg1911427
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283044, nssv14283046, nssv14283045
SamplesNA19238, HG00731, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3240659
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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