A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866160



Internal ID22641095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9716023..9729463hg38UCSC Ensembl
chr10:9757986..9771426hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813441
hg1913441
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866160
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