A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452385



Internal ID22510258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104600450..104604711hg38UCSC Ensembl
chr14:105066787..105071048hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg384262
hg194262
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866065
Supporting Variants
Samples
Known GenesTMEM179
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452385
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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