A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519367



Internal ID20892728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54230901..54241200hg38UCSC Ensembl
chr19:54734776..54745076hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3810300
hg1910301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200256
Samples
Known GenesLILRA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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