A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746110



Internal ID21389281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73109850..73112849hg38UCSC Ensembl
chr3:73159001..73162000hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434087
Supporting Variants
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746110
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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