A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180362



Internal ID20747402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94171801..94177300hg38UCSC Ensembl
chr11:93904967..93910466hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466093
Supporting Variants
Samples
Known GenesPANX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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