A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526426



Internal ID20899787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11608401..11610600hg38UCSC Ensembl
chr18:11608400..11610599hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182795
Samples
Known GenesSLC35G4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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