A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519418



Internal ID20892779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58488656..58504394hg38UCSC Ensembl
chr19:59000023..59015761hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3815739
hg1915739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049921
Samples
Known GenesSLC27A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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