A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17743019



Internal ID166685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56876388..56886838hg38UCSC Ensembl
chrY:59022535..59032985hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3810451
hg1910451
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17743019
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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