A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14261699



Internal ID22133616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:78612693..78634551hg38UCSC Ensembl
Outerchr18:76372693..76394551hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3821859
hg1921859
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213131
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14261699
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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