A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522679



Internal ID20896040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54233901..54241100hg38UCSC Ensembl
chr19:54737777..54744976hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200259
Samples
Known GenesLILRA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522679
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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