A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742963



Internal ID166629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22020088..22557281hg38UCSC Ensembl
chrY:24166235..24703428hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38537194
hg19537194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423602
Supporting Variants
Samples
Known GenesLOC100652931, PRY, PRY2, RBMY1F, RBMY1J, RBMY2FP, TTTY5, TTTY6, TTTY6B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742963
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00251731


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