A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522988



Internal ID20896349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38952157..38954820hg38UCSC Ensembl
chr19:39442797..39445460hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382664
hg192664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047831
Samples
Known GenesFBXO17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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