A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032481



Internal ID89344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16579223..16579266hg38UCSC Ensembl
chr10:16621222..16621265hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032481
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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