A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17856252



Internal ID22039895
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 StatusS
Merged Variantsnsv6255256
Supporting Variants
Samples
Known GenesIL2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17856252
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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