A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159811



Internal ID21471999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255276..133255331hg38UCSC Ensembl
chr9:136130663..136130718hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592110
Supporting Variants
SamplesHG03125
Known GenesABO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159811
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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