A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731119



Internal ID20507037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103999643..103999766hg38UCSC Ensembl
chr14:104465980..104466103hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264704
Samples
Known GenesTDRD9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731119
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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