A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421576



Internal ID200643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26523252..26598568hg38UCSC Ensembl
chrY:28669399..28744715hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3875317
hg1975317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421576
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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