A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14415607



Internal ID22151164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127466082..127466082hg38UCSC Ensembl
chr11:127335977..127335977hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3548509
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14415607
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer