A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753389



Internal ID20529249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71848773..71848773hg38UCSC Ensembl
chr10:73608530..73608530hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287373
Samples
Known GenesPSAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753389
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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