A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5545562



Internal ID319593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20066911..20096152hg38UCSC Ensembl
chrY:22228797..22258038hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3829242
hg1929242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5545562
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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