A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606387



Internal ID21554692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13234200..13234200hg38UCSC Ensembl
chr3:13275700..13275700hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135011
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606387
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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