A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236144



Internal ID22373498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:29243480..29296760hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14266518, nssv14266519, nssv14266520
SamplesNA19240, HG00733, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236144
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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