A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863741



Internal ID22638676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41580287..41582769hg38UCSC Ensembl
chr14:42049490..42051972hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382483
hg192483
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863741
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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