A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742960



Internal ID166626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21913281..22563281hg38UCSC Ensembl
chrY:24059428..24709428hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38650001
hg19650001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421434
Supporting Variants
Samples
Known GenesLOC100652931, PRY, PRY2, RBMY1B, RBMY1D, RBMY1E, RBMY1F, RBMY1J, RBMY2FP, TTTY5, TTTY6, TTTY6B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742960
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00251889


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