A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467280



Internal ID22525171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28380135..28400610hg38UCSC Ensembl
chr14:28849341..28869816hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3820476
hg1920476
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467280
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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