A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850900



Internal ID22625835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125908163..125909974hg38UCSC Ensembl
chr11:125778058..125779869hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454045, nssv17450850
Samples
Known GenesDDX25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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