A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609860



Internal ID21558165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26150928..26150928hg38UCSC Ensembl
chr2:26373797..26373797hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113947
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609860
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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