A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848204



Internal ID22623139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16375914..16390927hg38UCSC Ensembl
chr9:16375912..16390925hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3815014
hg1915014
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848204
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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