A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975527



Internal ID22750462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110929100..110929100hg38UCSC Ensembl
chr11:110799824..110799824hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975527
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