A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760260



Internal ID20536120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40894356..40894356hg38UCSC Ensembl
chr4:40896373..40896373hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283659
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760260
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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