A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134930



Internal ID20701970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90555322..90564205hg38UCSC Ensembl
chr5:89851139..89860022hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg388884
hg198884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413872
Supporting Variants
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134930
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