A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848817



Internal ID22623752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98985525..98992766hg38UCSC Ensembl
chr14:99451862..99459103hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387242
hg197242
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848817
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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