A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858978



Internal ID22042621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46779414..46779414hg38UCSC Ensembl
chr6:46747151..46747151hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858978
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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