A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516407



Internal ID20889768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14273501..14342700hg38UCSC Ensembl
chr18:14273500..14342699hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3869200
hg1969200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3299n223
Supporting Variantsnssv18188590
Samples
Known GenesCYP4F35P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516407
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