A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966371



Internal ID22741306
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 Variantsnssv17351751
Samples
Known GenesTECTB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966371
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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