A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742957



Internal ID166623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21543793..21549793hg38UCSC Ensembl
chrY:23705679..23711679hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138451
Supporting Variants
Samples
Known GenesRBMY1A1, RBMY1B, RBMY1D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742957
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.908373


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