A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109462



Internal ID21504110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1443666..1444536hg38UCSC Ensembl
chr2:1447438..1448308hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570945
Supporting Variants
SamplesNA19239
Known GenesTPO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109462
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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