A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469740



Internal ID22527630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89710111..89719469hg38UCSC Ensembl
chr14:90176455..90185813hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg389359
hg199359
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859552
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469740
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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