A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616350



Internal ID21564655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168792033..168792033hg38UCSC Ensembl
chr2:169648543..169648543hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110553
SamplesHG02011
Known GenesNOSTRIN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616350
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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