A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408238



Internal ID22466108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55783131..55783131hg38UCSC Ensembl
chr20:54358187..54358187hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408238
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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