A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255051



Internal ID22059661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100491596..100491596hg38UCSC Ensembl
chr4:101412753..101412753hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17855912
Samples
Known GenesEMCN
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255051
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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