A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579874



Internal ID21528358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116678863..116679583hg38UCSC Ensembl
chr8:117691102..117691822hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157744
SamplesHG00731
Known GenesEIF3H
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579874
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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