A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515951



Internal ID20889312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28511341..28511829hg38UCSC Ensembl
chr18:26091305..26091793hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515951
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