A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853114



Internal ID22628049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21606440..21608209hg38UCSC Ensembl
chr14:22074594..22076360hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381770
hg191767
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463944, nssv17464053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853114
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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