A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574341



Internal ID21766384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180650092..180658759hg38UCSC Ensembl
chr5:180077092..180085759hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg388668
hg198668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574341
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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