A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255256



Internal ID22059866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122452851..122452851hg38UCSC Ensembl
chr4:123374006..123374006hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856252
Samples
Known GenesIL2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255256
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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