A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231931



Internal ID20798971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5114119..5118549hg38UCSC Ensembl
chr6:5114353..5118783hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg384431
hg194431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414473
Supporting Variants
Samples
Known GenesLYRM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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