A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426276



Internal ID22484146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138196858..138197772hg38UCSC Ensembl
chr5:137532547..137533461hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898723
Supporting Variants
Samples
Known GenesCDC23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426276
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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