A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413101



Internal ID21070654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102490988..102565454hg38UCSC Ensembl
chr5:101826692..101901158hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3874467
hg1974467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214471
Samples
Known GenesSLCO6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413101
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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