A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459427



Internal ID22211798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925259hg38UCSC Ensembl
chr6:13925300..13925490hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3189564
Supporting Variants
SamplesHG00733
Known GenesRNF182
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459427
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer