A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862458



Internal ID22637393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75221608..75227573hg38UCSC Ensembl
chr14:75688311..75694276hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385966
hg195966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862458
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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