A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159845



Internal ID21510426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453494..113453664hg38UCSC Ensembl
chr9:116215774..116215944hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602702
Supporting Variants
SamplesNA24385
Known GenesRGS3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159845
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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