A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14262264



Internal ID22220764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:80629396..80645130hg38UCSC Ensembl
Outerchr17:78603196..78618930hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg389968
hg199968
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243702
Supporting Variants
SamplesHG00733
Known GenesRPTOR
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14262264
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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