A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14256076



Internal ID22189557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:132361394..132368104hg38UCSC Ensembl
Outerchr12:132937980..132944690hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3239282
Supporting Variants
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14256076
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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