A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609099



Internal ID21557404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12372553..12372553hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169589
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609099
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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