A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068316



Internal ID21490734
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 StatusS
Merged Variantsnsv5598821
Supporting Variants
SamplesNA19238
Known GenesRBM20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068316
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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