A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169466



Internal ID21512797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13984161..14058526hg38UCSC Ensembl
chrY:16096041..16170406hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3874366
hg1974366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665521
Supporting Variants
Samples
Known GenesVCY, VCY1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169466
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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