A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639437



Internal ID21587742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129699950..129699950hg38UCSC Ensembl
chr8:130712196..130712196hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148936
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639437
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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