A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327166



Internal ID20860303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169466408..169466725hg38UCSC Ensembl
chr1:169435646..169435963hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201645
Samples
Known GenesSLC19A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327166
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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