A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14411386



Internal ID22315626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6589667..6589776hg38UCSC Ensembl
chr5:6589780..6589889hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182743
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)nssv14411386
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