A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159342



Internal ID21427323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86694049..86694098hg38UCSC Ensembl
chr8:87706277..87706326hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572822
Supporting Variants
SamplesHG00731
Known GenesCNGB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159342
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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