A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850167



Internal ID22625102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92806518..92810870hg38UCSC Ensembl
chr9:95568800..95573152hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384353
hg194353
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514766
Samples
Known GenesANKRD19P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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