A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849456



Internal ID22033099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11056599..11056599hg38UCSC Ensembl
chr17:10959916..10959916hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849456
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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