A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517838



Internal ID20891199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56166407..56214121hg38UCSC Ensembl
chr19:56677776..56725490hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3847715
hg1947715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199668
Samples
Known GenesGALP, ZSCAN5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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