A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609933



Internal ID21558238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8176810..8176810hg38UCSC Ensembl
chr3:8218497..8218497hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134586
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609933
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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