A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129145



Internal ID21497873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147967510..147967510hg38UCSC Ensembl
chr3:147685297..147685297hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609048
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129145
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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