A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258927



Internal ID20468115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100873198..100873887hg38UCSC Ensembl
chr14:101339535..101340224hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16258927
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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