A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627029



Internal ID21575334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26078268..26078268hg38UCSC Ensembl
chr8:25935784..25935784hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142930, nssv17157321
SamplesHG00731, HG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627029
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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