A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977220



Internal ID22752155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6063349..6063349hg38UCSC Ensembl
chr20:6043995..6043995hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977220
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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