A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035198



Internal ID91200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70243859..70243910hg38UCSC Ensembl
chr10:72003615..72003666hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5400538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035198
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005932


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