A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650771



Internal ID21599076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108982839..108982839hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076551
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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