A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850493



Internal ID22625428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63981925..63984824hg38UCSC Ensembl
chr11:63749397..63752296hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850493
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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