A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865353



Internal ID22640288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98737201..98742826hg38UCSC Ensembl
chr14:99203538..99209163hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385626
hg195626
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865353
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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