A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639151



Internal ID21587456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127817528..127817528hg38UCSC Ensembl
chr8:128829774..128829774hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155932
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639151
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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