A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742829



Internal ID166495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19047824..19498360hg38UCSC Ensembl
chrY:21209710..21660246hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38450537
hg19450537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138184
Supporting Variants
Samples
Known GenesBCORP1, TTTY14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00601685


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