A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138451



Internal ID337635
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 StatusM
Merged Variants
Supporting Variantsnssv17742957
Samples
Known GenesRBMY1A1, RBMY1B, RBMY1D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138451
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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