A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159711



Internal ID21486208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121092467..121092542hg38UCSC Ensembl
chr9:123854745..123854820hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603564
Supporting Variants
SamplesNA12878
Known GenesCNTRL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159711
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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