A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971292



Internal ID22746227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44984150..45064699hg38UCSC Ensembl
chr15:45276348..45356897hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3880550
hg1980550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373999
Samples
Known GenesSORD
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971292
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