A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849927



Internal ID22624862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132811191..132817690hg38UCSC Ensembl
chr11:132681086..132687585hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454410
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849927
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