A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886866



Internal ID22661855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11681572..11686471hg38UCSC Ensembl
chr18:11681571..11686470hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886866
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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