A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738346



Internal ID162012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10208788..10220388hg38UCSC Ensembl
chrY:10046397..10057997hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3811601
hg1911601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425530
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738346
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00252048


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