A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738296



Internal ID161962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6245388..6267388hg38UCSC Ensembl
chrY:6113429..6135429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139057
Supporting Variants
Samples
Known GenesTSPY2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738296
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.993586


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