A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425292



Internal ID204259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14924123..14956123hg38UCSC Ensembl
chrY:17036003..17068003hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3832001
hg1932001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425292
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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