A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132834



Internal ID21506033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197030146..197030146hg38UCSC Ensembl
chr3:196757017..196757017hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613290
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132834
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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