A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198640



Internal ID22348339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58484702..58485927hg38UCSC Ensembl
chr15:58776901..58778126hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14418240
SamplesHG00514
Known GenesLIPC
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198640
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