A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14259118



Internal ID22193433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84635872..84637381hg38UCSC Ensembl
Outerchr15:85179103..85180612hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3232492
Supporting Variants
SamplesHG00731
Known GenesSCAND2P
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14259118
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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