A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069205



Internal ID21978438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24917401..24917401hg38UCSC Ensembl
chr7:24957020..24957020hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576834
Samples
Known GenesOSBPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069205
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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