A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853600



Internal ID22628535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110245751..110246850hg38UCSC Ensembl
chr9:113008031..113009130hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510707, nssv17510708
Samples
Known GenesTXN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853600
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