A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742989



Internal ID166655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26285281..26562388hg38UCSC Ensembl
chrY:28431428..28708535hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38277108
hg19277108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742989
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00503461


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