A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969561



Internal ID22744496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4398708..4642744hg38UCSC Ensembl
chr16:4448709..4692745hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38244037
hg19244037
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384875
Samples
Known GenesC16orf96, CDIP1, CORO7, CORO7-PAM16, DNAJA3, HMOX2, MGRN1, NMRAL1, UBALD1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969561
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