A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742995



Internal ID166661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26523252..26598568hg38UCSC Ensembl
chrY:28669399..28744715hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3875317
hg1975317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742995
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00313873


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