A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740363



Internal ID20516338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69408783..69408852hg38UCSC Ensembl
chr10:71168539..71168608hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296248
Samples
Known GenesTACR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740363
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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