A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868821



Internal ID22643756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62556360..62558524hg38UCSC Ensembl
chr20:61153567..61155731hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487316
Samples
Known GenesC20orf166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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