A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124510



Internal ID20691550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124069836..124082316hg38UCSC Ensembl
chr5:123405529..123418009hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3812481
hg1912481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124510
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