A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524590



Internal ID21848948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84558362..84558483hg38UCSC Ensembl
chr1:85024045..85024166hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984960
Supporting Variants
Samples
Known GenesCTBS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524590
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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