A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255759



Internal ID22060369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176692418..176692418hg38UCSC Ensembl
chr4:177613572..177613572hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856129
Samples
Known GenesVEGFC
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255759
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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