A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849138



Internal ID22624073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122530035..122543434hg38UCSC Ensembl
chr11:122400743..122414142hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849138
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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