A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136566



Internal ID21439620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25275286..25275610hg38UCSC Ensembl
chr5:25275395..25275719hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583648
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136566
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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