A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17113054



Internal ID21460799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3285770..3285883hg38UCSC Ensembl
chr2:3289541..3289654hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580636
Supporting Variants
SamplesHG02818
Known GenesTSSC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17113054
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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