A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643689



Internal ID21591994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124865383..124865383hg38UCSC Ensembl
chr8:125877625..125877625hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140214
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643689
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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