A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874238



Internal ID22649189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31622413..31650529hg38UCSC Ensembl
chr20:30210216..30238332hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3828117
hg1928117
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485282
Samples
Known GenesCOX4I2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874238
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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