A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533146



Internal ID21857502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59131751..59132017hg38UCSC Ensembl
chr1:59597423..59597689hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984457
Supporting Variants
Samples
Known GenesHSD52
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533146
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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