A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742962



Internal ID166628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21971281..21981281hg38UCSC Ensembl
chrY:24117428..24127428hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742962
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000653595


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