A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429221



Internal ID208072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17208123..17504123hg38UCSC Ensembl
chrY:19320003..19616003hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38296001
hg19296001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742819
Samples
Known GenesFAM41AY1, FAM41AY2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429221
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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