A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424962



Internal ID203936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9334371..9343388hg38UCSC Ensembl
chrY:9171980..9180997hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg389018
hg199018
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738333
Samples
Known GenesTTTY20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424962
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer