A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159631



Internal ID21493799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111984449..111984868hg38UCSC Ensembl
chr9:114746729..114747148hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592021
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159631
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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