A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866778



Internal ID22641713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33840022..33841321hg38UCSC Ensembl
chr11:33861568..33862867hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866778
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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