A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532141



Internal ID21856497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206923706..206924626hg38UCSC Ensembl
chr1:207097051..207097971hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532141
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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