A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742948



Internal ID166614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20941355..20947692hg38UCSC Ensembl
chrY:23103241..23109578hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg386338
hg196338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742948
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00187852


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