A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115425



Internal ID20682465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169657963..169658446hg38UCSC Ensembl
chr4:170579114..170579597hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382179
Supporting Variants
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00089


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