A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14418732



Internal ID22155536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119646882..119647038hg38UCSC Ensembl
chr11:119517592..119517748hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191402
Supporting Variants
SamplesHG00514
Known GenesPVRL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14418732
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