A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664665



Internal ID21612970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26512240..26515366hg38UCSC Ensembl
chrY:28658387..28661513hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg383127
hg193127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170487
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664665
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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