A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431709



Internal ID210476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:4973388..4983688hg38UCSC Ensembl
chrY:4841429..4851729hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3810301
hg1910301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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