A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575210



Internal ID21523637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94317433..94317738hg38UCSC Ensembl
chr8:95329661..95329966hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157875
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575210
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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