A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851498



Internal ID22626433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64764464..64765674hg38UCSC Ensembl
chr11:64531936..64533146hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458299
Samples
Known GenesSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851498
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