A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130395



Internal ID21512720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28414484..28420104hg38UCSC Ensembl
chr3:28455975..28461595hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg385621
hg195621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670743
Supporting Variants
Samples
Known GenesZCWPW2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130395
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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