A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742998



Internal ID166664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26615388..26620388hg38UCSC Ensembl
chrY:28761535..28766535hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742998
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002313


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