A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267073



Internal ID20476291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77220854..77220854hg38UCSC Ensembl
chr14:77687197..77687197hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765804
Supporting Variants
Samples
Known GenesTMEM63C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267073
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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