A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529379



Internal ID20902740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3708680..3711348hg38UCSC Ensembl
chr19:3708678..3711346hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382669
hg192669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046621
Samples
Known GenesTJP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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