A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419558



Internal ID198687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18452123..19040123hg38UCSC Ensembl
chrY:20614009..21202009hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38588001
hg19588001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742826
Samples
Known GenesCD24, HSFY1, HSFY2, NCRNA00185, TTTY14, TTTY9A, TTTY9B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419558
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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