A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118359



Internal ID20685399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55400101..55402900hg38UCSC Ensembl
chr4:56266268..56269067hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377891
Supporting Variants
Samples
Known GenesTMEM165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0309


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