A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360455



Internal ID21018008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48909410..48926653hg38UCSC Ensembl
chr3:48946843..48964086hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3817244
hg1917244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209346
Samples
Known GenesARIH2, ARIH2OS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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