A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854664



Internal ID22629599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60196079..60207241hg38UCSC Ensembl
chr14:60662797..60673959hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3811163
hg1911163
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854664
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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