A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364232



Internal ID22589901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13370403..13370983hg38UCSC Ensembl
chr10:13412403..13412983hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364232
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005


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