A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357114



Internal ID21014667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170507097..170593904hg38UCSC Ensembl
chr3:170224886..170311693hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3886808
hg1986808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209210
Samples
Known GenesSLC7A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357114
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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