A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643280



Internal ID21591585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112304736..112304736hg38UCSC Ensembl
chr10:114064494..114064494hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068516
SamplesNA19239
Known GenesTECTB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643280
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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