A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186965



Internal ID20754005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131915001..131920100hg38UCSC Ensembl
chr10:133728505..133733604hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453821
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00011


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