A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973006



Internal ID22747941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23334189..23334189hg38UCSC Ensembl
chr20:23314826..23314826hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973006
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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