A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430138



Internal ID208959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:4357288..4635388hg38UCSC Ensembl
chrY:4225329..4503429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38278101
hg19278101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430138
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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