A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622317



Internal ID21570622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67300522..67300522hg38UCSC Ensembl
chr3:67350946..67350946hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119969
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622317
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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