A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975824



Internal ID51278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152785956..152793537hg38UCSC Ensembl
chr5:152165516..152173097hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg387582
hg197582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975824
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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