A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530497



Internal ID20903858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4164880..4168101hg38UCSC Ensembl
chr19:4164877..4168098hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383222
hg193222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046365
Samples
Known GenesCREB3L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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