A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766725



Internal ID20542585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69228536..69228536hg38UCSC Ensembl
chr7:68693523..68693523hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766725
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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