A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849294



Internal ID22624229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102258933..102259932hg38UCSC Ensembl
chr9:105021215..105022214hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849294
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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