A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742990



Internal ID166656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26355096..26456684hg38UCSC Ensembl
chrY:28501243..28602831hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38101589
hg19101589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742990
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00250941


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