A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640189



Internal ID21588494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74591312..74591312hg38UCSC Ensembl
chr8:75503547..75503547hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147853
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640189
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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