A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032449



Internal ID89328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14568309..14568719hg38UCSC Ensembl
chr10:14610308..14610718hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475006
Supporting Variants
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032449
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.481611


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