A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598821



Internal ID21547450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110766861..110766986hg38UCSC Ensembl
chr10:112526619..112526744hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068316
SamplesNA19238
Known GenesRBM20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598821
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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