A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279403



Internal ID20488621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117046417..117051817hg38UCSC Ensembl
chr5:116382113..116387513hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733250
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279403
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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