A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353637



Internal ID22579306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92059325..92059325hg38UCSC Ensembl
chr10:93819082..93819082hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956227
Supporting Variants
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353637
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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