A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617112



Internal ID21565417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17853106..17853106hg38UCSC Ensembl
chr2:18034373..18034373hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110728
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617112
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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