A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069907



Internal ID21481759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18208764..18208764hg38UCSC Ensembl
chr10:18497693..18497693hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641895
Supporting Variants
SamplesHG03683
Known GenesCACNB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069907
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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