A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758904



Internal ID20534764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19859896..19859896hg38UCSC Ensembl
chr11:19881442..19881442hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269494
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758904
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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