A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644453



Internal ID21592758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116601257..116601257hg38UCSC Ensembl
chr9:119363536..119363536hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160274
SamplesNA12329
Known GenesASTN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644453
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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