A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065477



Internal ID21511622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58593944..58594268hg38UCSC Ensembl
chr1:59059616..59059940hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565076
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065477
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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