A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137382



Internal ID21459449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153925758..153925758hg38UCSC Ensembl
chr3:153643547..153643547hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617953
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137382
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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