A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671118



Internal ID21619423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89596698..89653322hg38UCSC Ensembl
chr16:89663106..89719730hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3856625
hg1956625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083058
Samples
Known GenesCHMP1A, CPNE7, DPEP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671118
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer