A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982352



Internal ID21891695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206924250..206924318hg38UCSC Ensembl
chr1:207097595..207097663hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982352
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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