A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641575



Internal ID21589880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89371445..89371445hg38UCSC Ensembl
chr9:91986360..91986360hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163127
SamplesNA12329
Known GenesSEMA4D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641575
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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