A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528249



Internal ID20901610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23277758..23306503hg38UCSC Ensembl
chr18:20857722..20886467hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3828746
hg1928746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189624
Samples
Known GenesTMEM241
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528249
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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