A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159625



Internal ID21493800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111869466..111869784hg38UCSC Ensembl
chr9:114631746..114632064hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603673
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159625
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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