A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642238



Internal ID21590543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95374841..95374841hg38UCSC Ensembl
chr9:98137123..98137123hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163775
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642238
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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