A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867369



Internal ID22642304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97215601..97217319hg38UCSC Ensembl
chr9:99977883..99979601hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381719
hg191719
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514964, nssv17514963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867369
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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