A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971417



Internal ID48289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98031003..98031088hg38UCSC Ensembl
chr5:97366707..97366792hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971417
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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