A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389234



Internal ID22447104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21558148..21568150hg38UCSC Ensembl
chr14:22026279..22036281hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3810003
hg1910003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389234
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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