A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225904



Internal ID22368896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:78612693..78661272hg38UCSC Ensembl
Outerchr18:76372693..76421272hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3848580
hg1948580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14261782
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225904
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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