A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563908



Internal ID336834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20754592..20756191hg38UCSC Ensembl
chrY:22916478..22918077hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742945
Samples
Known GenesRPS4Y2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563908
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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