A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857667



Internal ID22632602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62171061..62173988hg38UCSC Ensembl
chr11:61938533..61941460hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382928
hg192928
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857667
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