A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350747



Internal ID22576416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52643568..52643755hg38UCSC Ensembl
chr10:54403328..54403515hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350747
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008


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