A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742955



Internal ID166621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21375793..21531793hg38UCSC Ensembl
chrY:23537679..23693679hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38156001
hg19156001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430674
Supporting Variants
Samples
Known GenesCYorf17, RBMY1A1, RBMY1B, RBMY1D, RBMY1E, RBMY2EP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742955
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00188561


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