A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409825



Internal ID22467695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65142182..65145679hg38UCSC Ensembl
chr4:66007900..66011397hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg383498
hg193498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409825
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