A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962533



Internal ID42333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10501225..10502127hg38UCSC Ensembl
chr5:10501337..10502239hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458258
Supporting Variants
Samples
Known GenesLOC101929412
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962533
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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