A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161394



Internal ID21457244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19145057..19209866hg38UCSC Ensembl
chr9:19145055..19209864hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3864810
hg1964810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587435
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161394
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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