A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615060



Internal ID21563365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11275679..11275679hg38UCSC Ensembl
chrY:13431355..13431355hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168818
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615060
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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