A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848822



Internal ID22623757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31693936..31698885hg38UCSC Ensembl
chr14:32163142..32168091hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459498
Samples
Known GenesNUBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848822
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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