A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748754



Internal ID20524781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92400101..92409596hg38UCSC Ensembl
chr10:94159858..94169353hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389496
hg199496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748754
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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