A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665002



Internal ID21613307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1674234..1677287hg38UCSC Ensembl
chrY:1743127..1746180hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg383054
hg193054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169943
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665002
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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