A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128628



Internal ID20695668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150019086..150027801hg38UCSC Ensembl
chr5:149398649..149407364hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg388716
hg198716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415189
Supporting Variants
Samples
Known GenesHMGXB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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