A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850876



Internal ID22625811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57520282..57523092hg38UCSC Ensembl
chr11:57287755..57290565hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850876
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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