A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406068



Internal ID21063621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54061408..54098361hg38UCSC Ensembl
chr5:53357238..53394191hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3836954
hg1936954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214029
Samples
Known GenesARL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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