A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122484



Internal ID21483270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27214823..27214823hg38UCSC Ensembl
chr3:27256314..27256314hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605850
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122484
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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