A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181136



Internal ID20748176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28396392..28397316hg38UCSC Ensembl
chr10:28685321..28686245hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181136
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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