A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563029



Internal ID335967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97293370..97293402hg38UCSC Ensembl
chr9:100055652..100055684hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027556
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563029
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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