A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738277



Internal ID161943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3844388..3853388hg38UCSC Ensembl
chrY:3712429..3721429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738277
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000626959


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