A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848059



Internal ID22031702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5054101..5054101hg38UCSC Ensembl
chr17:4957396..4957396hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848059
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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