A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749281



Internal ID21386386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24377365..24379364hg38UCSC Ensembl
chr20:24358001..24360000hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433256
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749281
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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