A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533763



Internal ID20907124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5958686..6600700hg38UCSC Ensembl
chr18:5958685..6600699hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38642015
hg19642015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181544
Samples
Known GenesC18orf64, L3MBTL4, MIR4317
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer