A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493377



Internal ID22551306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24796251..24799361hg38UCSC Ensembl
chr4:24797873..24800983hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383111
hg193111
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839519
Supporting Variants
Samples
Known GenesSOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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