A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046624



Internal ID20613664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3710120..3726470hg38UCSC Ensembl
chr19:3710118..3726468hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3816351
hg1916351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522448
Supporting Variants
Samples
Known GenesTJP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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