A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14425802



Internal ID22165870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24683759..24684456hg38UCSC Ensembl
chr6:24683987..24684684hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183189
Supporting Variants
SamplesHG00514
Known GenesACOT13
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14425802
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