A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156018



Internal ID21509153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20739738..20743351hg38UCSC Ensembl
chr8:20597249..20600862hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383614
hg193614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568489
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156018
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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