A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868279



Internal ID22643214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62166720..62171669hg38UCSC Ensembl
chr20:60741776..60746725hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487307, nssv17487308
Samples
Known GenesSS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868279
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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