A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421908



Internal ID21079461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47984416..48025822hg38UCSC Ensembl
chr8:48896976..48938382hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3841407
hg1941407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225961
Samples
Known GenesUBE2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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