A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752071



Internal ID20527931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127720797..127720797hg38UCSC Ensembl
chr9:130483076..130483076hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283087
Samples
Known GenesTTC16
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752071
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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