A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382207



Internal ID22440077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54151912..54163793hg38UCSC Ensembl
chr14:54618630..54630511hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3811882
hg1911882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382207
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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