A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192059



Internal ID20759099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103526943..103562781hg38UCSC Ensembl
chr14:103993280..104029118hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3835839
hg1935839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514597
Supporting Variants
Samples
Known GenesBAG5, TRMT61A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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