A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126771



Internal ID21506913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129914165..129916093hg38UCSC Ensembl
chr3:129633008..129634936hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381929
hg191929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573285
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126771
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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