A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518892



Internal ID20892253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16546497..16552534hg38UCSC Ensembl
chr19:16657308..16663345hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg386038
hg196038
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197672
Samples
Known GenesSLC35E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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