A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132521



Internal ID21442987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33478654..33478720hg38UCSC Ensembl
chr5:33478759..33478825hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571683
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132521
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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