A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922392



Internal ID22697617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92720337..92724884hg38UCSC Ensembl
chr11:92453503..92458050hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384548
hg194548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357487
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922392
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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