A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534030



Internal ID20907391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38634478..38647051hg38UCSC Ensembl
chr19:39125118..39137691hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3812574
hg1912574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198105
Samples
Known GenesEIF3K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534030
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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