A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369001



Internal ID21026554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141838485..141882768hg38UCSC Ensembl
chr3:141557327..141601610hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3844284
hg1944284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209646
Samples
Known GenesATP1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369001
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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