A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845163



Internal ID22620098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18010486..18011605hg38UCSC Ensembl
chr6:18010717..18011836hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503703, nssv17503702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845163
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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