A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6243706



Internal ID22048316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3025886..3025886hg38UCSC Ensembl
chr4:3027613..3027613hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17855017
Samples
Known GenesGRK4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6243706
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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