A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738286



Internal ID161952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5080388..5091388hg38UCSC Ensembl
chrY:4948429..4959429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3811001
hg1911001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415066
Supporting Variants
Samples
Known GenesPCDH11Y
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738286
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00314663


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