A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954452



Internal ID22729696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84512388..84512388hg38UCSC Ensembl
chr10:86272144..86272144hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351431
Samples
Known GenesCCSER2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954452
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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