A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977490



Internal ID22752425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2546043..2628645hg38UCSC Ensembl
chr9:2546043..2628645hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3882603
hg1982603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434273
Samples
Known GenesFLJ35024, VLDLR
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977490
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