A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613095



Internal ID21561400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27282548..27282548hg38UCSC Ensembl
chr3:27324039..27324039hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137930
SamplesHG02492
Known GenesNEK10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613095
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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