A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606879



Internal ID21555184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31433343..31433343hg38UCSC Ensembl
chr3:31474835..31474835hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130975
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606879
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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