A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855309



Internal ID22630244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43871938..43877837hg38UCSC Ensembl
chr14:44341141..44347040hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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