A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854013



Internal ID22628948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94687950..94712975hg38UCSC Ensembl
chr14:95154287..95179312hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3825026
hg1925026
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854013
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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