A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983006



Internal ID21892349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23413476..23418356hg38UCSC Ensembl
chr1:23739969..23744849hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384881
hg194881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522339
Samples
Known GenesTCEA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983006
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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