A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519965



Internal ID20893326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46387657..46391429hg38UCSC Ensembl
chr18:43967620..43971392hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg383773
hg193773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041912
Samples
Known GenesRNF165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519965
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