A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294712



Internal ID20503930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86909217..86909217hg38UCSC Ensembl
chr14:87375561..87375561hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763272
Supporting Variants
Samples
Known GenesLOC283585
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294712
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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