A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852393



Internal ID22627328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58188313..58193660hg38UCSC Ensembl
chr11:57955785..57961132hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg385348
hg195348
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459381
Samples
Known GenesOR9Q2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852393
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