A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046291



Internal ID20613331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3548782..3566804hg38UCSC Ensembl
chr19:3548780..3566802hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3818023
hg1918023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522673
Supporting Variants
Samples
Known GenesMFSD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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