A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17113028



Internal ID21412058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:242163784..242168424hg38UCSC Ensembl
chr16:90285395..90290031hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg384641
hg194637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583306
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17113028
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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