A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129181



Internal ID21416400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134329150..134329150hg38UCSC Ensembl
chr3:134047992..134047992hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611937
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129181
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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