A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640879



Internal ID21589184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87845036..87845036hg38UCSC Ensembl
chr9:90459951..90459951hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382812
hg192812
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163209
SamplesHG00512
Known GenesCTSLP8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640879
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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