A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521038



Internal ID20894399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45005707..45010781hg38UCSC Ensembl
chr19:45508965..45514039hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385075
hg195075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198863
Samples
Known GenesRELB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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