A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136646



Internal ID20703686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109781778..109795095hg38UCSC Ensembl
chr6:110102981..110116298hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3813318
hg1913318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618366
Supporting Variants
Samples
Known GenesFIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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