A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17856503



Internal ID22040146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115146526..115146526hg38UCSC Ensembl
chr1:115689147..115689147hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17856503
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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