A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3277832



Internal ID22377874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92768730..92768886hg38UCSC Ensembl
chr15:93311960..93312116hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV sva deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460309, nssv14405408
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsAbsence of a SVA mobile element insertion that is present in the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3277832
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer