A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261198



Internal ID22065808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24811405..24811405hg38UCSC Ensembl
chr7:24851024..24851024hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859939
Samples
Known GenesOSBPL3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261198
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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