A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120757



Internal ID21401228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139416423..139416423hg38UCSC Ensembl
chr3:139135265..139135265hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386050
hg196050
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623639
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120757
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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