A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380176



Internal ID22438046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22867959..22868658hg38UCSC Ensembl
chr14:23337168..23337867hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380176
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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