A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14262427



Internal ID22133886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:37778421..37783783hg38UCSC Ensembl
Outerchr18:35358385..35363747hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3238486
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14262427
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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