A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856854



Internal ID22631789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110581070..110586655hg38UCSC Ensembl
chr9:113343350..113348935hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385586
hg195586
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510762, nssv17510763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856854
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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