A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521376



Internal ID20894737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18251373..18252854hg38UCSC Ensembl
chr19:18362183..18363664hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381482
hg191482
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197722
Samples
Known GenesLOC729966
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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