A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855973



Internal ID22039616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86358366..86358366hg38UCSC Ensembl
chr1:86824049..86824049hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244307
Supporting Variants
Samples
Known GenesODF2L
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855973
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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