A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063496



Internal ID21972729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24979853..24979853hg38UCSC Ensembl
chr7:25019472..25019472hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566120
Samples
Known GenesOSBPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063496
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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