A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409959



Internal ID22467829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147402341..147402652hg38UCSC Ensembl
chr5:146781904..146782215hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890408
Supporting Variants
Samples
Known GenesDPYSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409959
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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