A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268708



Internal ID20835748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151203495..151203833hg38UCSC Ensembl
chr5:150583056..150583394hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568816
Supporting Variants
Samples
Known GenesCCDC69
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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