A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525757



Internal ID20899118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4841041..4873416hg38UCSC Ensembl
chr20:4821687..4854062hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832376
hg1932376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202945
Samples
Known GenesSLC23A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525757
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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