A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600913



Internal ID21792960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102877199..102877269hg38UCSC Ensembl
chr14:103343536..103343606hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026115
Supporting Variants
Samples
Known GenesTRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600913
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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