A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123606



Internal ID21464702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25783480..25783480hg38UCSC Ensembl
chr3:25824971..25824971hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605861
Supporting Variants
SamplesHG03065
Known GenesNGLY1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123606
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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