A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385651



Internal ID22299860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1009328..1009383hg38UCSC Ensembl
chr10:1055268..1055323hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199646
Supporting Variants
SamplesNA19240
Known GenesGTPBP4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385651
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