A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380301



Internal ID22438171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22449115..22535558hg38UCSC Ensembl
chr14:22918107..23004506hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3886444
hg1986400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380301
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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