A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16972674



Internal ID49149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116701607..116701736hg38UCSC Ensembl
chr5:116037303..116037432hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16972674
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.014049


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