A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972862



Internal ID22747797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148985738..148987102hg38UCSC Ensembl
chr3:148703525..148704889hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381365
hg191365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417028
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972862
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