A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292986



Internal ID20502204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100344958..100344958hg38UCSC Ensembl
chr14:100811295..100811295hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765742
Supporting Variants
Samples
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292986
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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