A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033457



Internal ID89992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28906500..28906551hg38UCSC Ensembl
chr10:29195429..29195480hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5404541
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033457
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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