A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861231



Internal ID22636166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81581879..81586678hg38UCSC Ensembl
chr11:81292921..81297720hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861231
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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