A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161517



Internal ID21453978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27444226..27444226hg38UCSC Ensembl
chr9:27444224..27444224hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626182
Supporting Variants
SamplesHG02011
Known GenesMOB3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161517
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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