A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975684



Internal ID51184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153090545..153091757hg38UCSC Ensembl
chr5:152470105..152471317hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381213
hg191213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975684
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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