A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121488



Internal ID21507179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138196835..138197749hg38UCSC Ensembl
chr5:137532524..137533438hg19UCSC 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 Variantsnsv5579529
Supporting Variants
SamplesNA19983
Known GenesCDC23
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121488
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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