A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356005



Internal ID21013558
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 StatusM
Merged Variants
Supporting Variantsnssv18209648
Samples
Known GenesATP1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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