A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752286



Internal ID20528146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123881228..123881228hg38UCSC Ensembl
chr10:125640744..125640744hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271813
Samples
Known GenesCPXM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752286
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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