A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405182



Internal ID21062735
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 StatusM
Merged Variants
Supporting Variantsnssv18215934
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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