A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180406



Internal ID20747446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129816577..129817200hg38UCSC Ensembl
chr11:129686472..129687095hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463799
Supporting Variants
Samples
Known GenesTMEM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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