A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633730



Internal ID21582035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108131543..108131543hg38UCSC Ensembl
chr9:110893823..110893823hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157344
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633730
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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