A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110394



Internal ID21494727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166191672..166191733hg38UCSC Ensembl
chr2:167048182..167048243hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578223
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110394
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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