A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667242



Internal ID21615549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18184807..18184995hg38UCSC Ensembl
chrY:20346693..20346881hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169870
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667242
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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