A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464569



Internal ID22522456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21540279..21543330hg38UCSC Ensembl
chr14:22008419..22011476hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383052
hg193058
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858332
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464569
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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