A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631865



Internal ID21580170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89159080..89159080hg38UCSC Ensembl
chr9:91773995..91773995hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386091
hg196091
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163115
SamplesHG02587
Known GenesSHC3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631865
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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