A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742971



Internal ID166637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22607281..22615388hg38UCSC Ensembl
chrY:24753428..24761535hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg388108
hg198108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742971
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00143575


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