A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859897



Internal ID22043540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153045876..153045876hg38UCSC Ensembl
chr6:153367011..153367011hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257367
Supporting Variants
Samples
Known GenesRGS17
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859897
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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