A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16973384



Internal ID49637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122162593..122163002hg38UCSC Ensembl
chr5:121498288..121498697hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457691
Supporting Variants
Samples
Known GenesLOC100505841
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16973384
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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