A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856382



Internal ID22631317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27308644..27321198hg38UCSC Ensembl
chr11:27330191..27342745hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3812555
hg1912555
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856382
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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