A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358276



Internal ID22583945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101731515..101745348hg38UCSC Ensembl
chr10:103491272..103505105hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3813834
hg1913834
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358276
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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