A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863379



Internal ID22638314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97088858..97093003hg38UCSC Ensembl
chr9:99851140..99855285hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg384146
hg194146
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863379
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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