A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469776



Internal ID22527666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93417671..93422450hg38UCSC Ensembl
chr14:93884017..93888796hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg384780
hg194780
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849904
Supporting Variants
Samples
Known GenesUNC79
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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