A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255478



Internal ID22060088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146953946..146953946hg38UCSC Ensembl
chr4:147875098..147875098hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255478
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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