A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650175



Internal ID21598480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72133584..72133584hg38UCSC Ensembl
chr11:71844630..71844630hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075836
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650175
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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