A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215934



Internal ID20782974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160670993..160682866hg38UCSC Ensembl
chr5:160098000..160109873hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811874
hg1911874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405182
Supporting Variants
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215934
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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