A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179515



Internal ID20746555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104811653..105834977hg38UCSC Ensembl
chr10:106571411..107594735hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381023325
hg191023325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451417
Supporting Variants
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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