A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864236



Internal ID22639171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104599132..104604135hg38UCSC Ensembl
chr9:107361413..107366416hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385004
hg195004
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510539, nssv17510538
Samples
Known GenesOR13C5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864236
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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