A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852306



Internal ID22627241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65562674..65580594hg38UCSC Ensembl
chr9:44839436..44857427hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3817921
hg1917992
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514032, nssv17514031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852306
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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