A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633634



Internal ID21581939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92813084..92813084hg38UCSC Ensembl
chr8:93825312..93825312hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144767
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633634
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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