A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867123



Internal ID22642058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122839674..122844723hg38UCSC Ensembl
chr9:125601953..125607002hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385050
hg195050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2190n209
Supporting Variantsnssv17511262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867123
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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