A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640027



Internal ID21588332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134905793..134905793hg38UCSC Ensembl
chr9:137797639..137797639hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160672
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640027
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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