A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291964



Internal ID20501182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82000027..82000090hg38UCSC Ensembl
chr14:82466371..82466434hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291964
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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