A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608299



Internal ID21556604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16538202..16538202hg38UCSC Ensembl
chr3:16579709..16579709hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126220
SamplesNA20847
Known GenesLINC00690
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608299
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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