A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121556



Internal ID21489499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130201575..130201575hg38UCSC Ensembl
chr3:129920418..129920418hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382958
hg192958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616186
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121556
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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