A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745894



Internal ID21385811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21721363..21722362hg38UCSC Ensembl
chr20:21702001..21703000hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433250
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745894
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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