A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14268264



Internal ID22258939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:47378553..47387881hg38UCSC Ensembl
Outerchr22:47774303..47783631hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383224
hg193224
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231205
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14268264
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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