A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527039



Internal ID20900400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49017701..49024300hg38UCSC Ensembl
chr19:49520958..49527557hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198227
Samples
Known GenesCGB, LOC101059948
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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