A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610063



Internal ID21558368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65172430..65172430hg38UCSC Ensembl
chr3:65158105..65158105hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123331
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610063
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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