A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463667



Internal ID22230128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144345099..144345207hg38UCSC Ensembl
chr6:144666235..144666343hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3178148
Supporting Variants
SamplesHG00733
Known GenesUTRN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14463667
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