A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619040



Internal ID21567345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18500799..18500799hg38UCSC Ensembl
chrY:20662685..20662685hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169895
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619040
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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