A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528533



Internal ID20901894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3711001..3717469hg38UCSC Ensembl
chr19:3710999..3717467hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386469
hg196469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046625
Samples
Known GenesTJP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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