A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533929



Internal ID20907290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62877748..62882550hg38UCSC Ensembl
chr18:60544981..60549783hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg384803
hg194803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043383
Samples
Known GenesPHLPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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