A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738423



Internal ID162089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13112123..13196123hg38UCSC Ensembl
chrY:15224037..15308021hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3884001
hg1983985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738423
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00251414


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