A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522653



Internal ID20896014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6436643..6442642hg38UCSC Ensembl
chr19:6436654..6442653hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198987
Samples
Known GenesSLC25A23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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