A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744982



Internal ID20520986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110224800..110224908hg38UCSC Ensembl
chr10:111984558..111984666hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293068
Samples
Known GenesMXI1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744982
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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