A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737924



Internal ID20513889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3752752..3753033hg38UCSC Ensembl
chr10:3794944..3795225hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737924
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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