A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523841



Internal ID20897202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38106162..38106530hg38UCSC Ensembl
chr18:35686126..35686494hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523841
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