A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617451



Internal ID21809498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27169399..27348355hg38UCSC Ensembl
chr14:27638605..27817561hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38178957
hg19178957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617451
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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