A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089376



Internal ID21440645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24479267..24479354hg38UCSC Ensembl
chr16:24490588..24490675hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597631
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089376
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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