A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17683722



Internal ID107388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12847106..12847157hg38UCSC Ensembl
chr10:12889106..12889157hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17683722
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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