A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613290



Internal ID21561595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197030146..197030146hg38UCSC Ensembl
chr3:196757017..196757017hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132834
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613290
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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