A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738333



Internal ID161999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9334371..9343388hg38UCSC Ensembl
chrY:9171980..9180997hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg389018
hg199018
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424962
Supporting Variants
Samples
Known GenesTTTY20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738333
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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