A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276163



Internal ID20485381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91836575..91836575hg38UCSC Ensembl
chr14:92302919..92302919hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759685
Supporting Variants
Samples
Known GenesTC2N
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276163
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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