A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516849



Internal ID20890210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:51839622..51841066hg38UCSC Ensembl
chr18:49365992..49367436hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381445
hg191445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516849
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