A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845743



Internal ID22029386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20315164..20315164hg38UCSC Ensembl
chr14:20783323..20783323hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249656
Supporting Variants
Samples
Known GenesCCNB1IP1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845743
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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