A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381224



Internal ID22286470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175302712..175302982hg38UCSC Ensembl
chr1:175271848..175272118hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182390
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381224
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