A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086463



Internal ID21403399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67465302..67465452hg38UCSC Ensembl
chr14:67932019..67932169hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593921
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086463
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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