A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763986



Internal ID20539846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2546960..2546960hg38UCSC Ensembl
chr7:2586594..2586594hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265121
Samples
Known GenesBRAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763986
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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