A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361211



Internal ID22586880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130684322..130767830hg38UCSC Ensembl
chr10:132482586..132566094hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3883509
hg1983509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361211
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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