A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706821



Internal ID21379097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142677037..142677374hg38UCSC Ensembl
chr2:143434606..143434943hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389966
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706821
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.758621


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