A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746938



Internal ID20522954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28506980..28507295hg38UCSC Ensembl
chr10:28795909..28796224hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746938
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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