A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848064



Internal ID22031707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5516084..5516084hg38UCSC Ensembl
chr17:5419404..5419404hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250579
Supporting Variants
Samples
Known GenesNLRP1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848064
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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