A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616177



Internal ID21564482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13450029..13450029hg38UCSC Ensembl
chr3:13491529..13491529hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125076
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616177
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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