A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738334



Internal ID162000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9397388..9403388hg38UCSC Ensembl
chrY:9234997..9240997hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421551
Supporting Variants
Samples
Known GenesTSPY10, TSPY3, TSPY4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738334
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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