A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639531



Internal ID21587836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97928912..97928912hg38UCSC Ensembl
chr9:100691194..100691194hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163425
SamplesNA19983
Known GenesHEMGN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639531
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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