A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14457392



Internal ID22251458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72170384..72170752hg38UCSC Ensembl
chr15:72462725..72463093hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198711
Supporting Variants
SamplesHG00733
Known GenesGRAMD2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14457392
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