A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv462n152



Internal ID22816165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169554159..169554257hg38UCSC Ensembl
chr1:169523397..169523495hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3171817, nsv3176908
SamplesNA19240, HG00733
Known GenesF5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv462n152
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