A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764355



Internal ID20540215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124141247..124141247hg38UCSC Ensembl
chr7:123781301..123781301hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764355
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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