A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763335



Internal ID20539195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15488707..15488707hg38UCSC Ensembl
chr9:15488705..15488705hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291288
Samples
Known GenesPSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763335
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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