A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848874



Internal ID22032517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56516984..56516984hg38UCSC Ensembl
chr17:54594345..54594345hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848874
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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