A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742959



Internal ID166625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21657937..21658102hg38UCSC Ensembl
chrY:23819823..23819988hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742959
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.009062


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