A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975780



Internal ID51248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151652821..151653005hg38UCSC Ensembl
chr5:151032382..151032566hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471283
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975780
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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