A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764701



Internal ID20540561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87845044..87845044hg38UCSC Ensembl
chr9:90459959..90459959hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382621
hg192621
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261781
Samples
Known GenesCTSLP8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764701
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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