A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280984



Internal ID20490202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179693342..179693476hg38UCSC Ensembl
chr5:179120343..179120477hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743556
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280984
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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