A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461878



Internal ID22229648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157804229..157804604hg38UCSC Ensembl
chr6:158225261..158225636hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3187118
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14461878
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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