A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614411



Internal ID21562716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202995223..202995223hg38UCSC Ensembl
chr2:203859946..203859946hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg381996
hg191996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111151
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614411
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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