A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638783



Internal ID21587088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133382579..133382579hg38UCSC Ensembl
chr9:136249451..136249451hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159975
SamplesHG02818
Known GenesC9orf96
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638783
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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