A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928012



Internal ID22703246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57493271..57493508hg38UCSC Ensembl
chr14:57959989..57960226hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378425
Samples
Known GenesC14orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928012
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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