A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032294



Internal ID89229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26384136..26384187hg38UCSC Ensembl
chr10:26673065..26673116hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383798
hg193798
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558249
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032294
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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