A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451120



Internal ID22246191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105454682..105454858hg38UCSC Ensembl
chr3:105173526..105173702hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3172616
Supporting Variants
SamplesHG00733
Known GenesALCAM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14451120
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