A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124016



Internal ID20691057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105850543..105850991hg38UCSC Ensembl
chr5:105186244..105186692hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414098
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00069


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