A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209648



Internal ID20776688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141875001..141878300hg38UCSC Ensembl
chr3:141593843..141597142hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356005
Supporting Variants
Samples
Known GenesATP1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209648
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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