A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934071



Internal ID22709390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57468565..57470463hg38UCSC Ensembl
chr14:57935283..57937181hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374325
Samples
Known GenesC14orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934071
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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