A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163409



Internal ID21488135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97236739..97245904hg38UCSC Ensembl
chr9:99999021..100008186hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg389166
hg199166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600040
Supporting Variants
SamplesNA18534
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163409
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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