A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652205



Internal ID21600510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98923693..98923693hg38UCSC Ensembl
chr15:99466922..99466922hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084027
SamplesHG00864
Known GenesIGF1R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652205
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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