A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711421



Internal ID135087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11060901..11060952hg38UCSC Ensembl
chr17:10964218..10964269hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711421
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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