A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760718



Internal ID20536579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111387145..111387145hg38UCSC Ensembl
chr9:114149425..114149425hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294912
Samples
Known GenesKIAA0368
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760718
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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