A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526815



Internal ID20900176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48602527..48617272hg38UCSC Ensembl
chr19:49105784..49120529hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3814746
hg1914746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3677n223
Supporting Variantsnssv18199590
Samples
Known GenesFAM83E, RPL18, SPACA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526815
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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