A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600141



Internal ID21792188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18212566..18214351hg38UCSC Ensembl
chrUn_gl000212:41318..43103hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381786
hg191786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600141
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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