A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967771



Internal ID22742707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72171325..72175177hg38UCSC Ensembl
chr15:72463666..72467518hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381482
Samples
Known GenesGRAMD2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967771
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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