A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200323



Internal ID22349792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73191319..73191503hg38UCSC Ensembl
chr15:73483660..73483844hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455296
SamplesHG00733
Known GenesNEO1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200323
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