A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840559



Internal ID22615494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99525776..99539906hg38UCSC Ensembl
chr4:100446933..100461063hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3814131
hg1914131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498667
Samples
Known GenesC4orf17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840559
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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