A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498177



Internal ID22556112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108627043..108647207hg38UCSC Ensembl
chr4:109548199..109568363hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3820165
hg1920165
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837286
Supporting Variants
Samples
Known GenesRPL34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498177
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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