A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616160



Internal ID21564465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62926315..62926315hg38UCSC Ensembl
chr3:62911990..62911990hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132124
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616160
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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