A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137594



Internal ID21510132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149706417..149706417hg38UCSC Ensembl
chr3:149424204..149424204hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622316
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137594
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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