A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975683



Internal ID51183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153089239..153089395hg38UCSC Ensembl
chr5:152468799..152468955hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975683
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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