A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518966



Internal ID20892327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30796565..30798838hg38UCSC Ensembl
chr19:31287472..31289745hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg382274
hg192274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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