A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030209



Internal ID87852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12882963..12882992hg38UCSC Ensembl
chr10:12924963..12924992hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030209
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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