A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209549



Internal ID20776589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112510201..112515800hg38UCSC Ensembl
chr4:113431357..113436956hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376773
Supporting Variants
Samples
Known GenesNEUROG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209549
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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