A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459849



Internal ID21117402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82693921..82717706hg38UCSC Ensembl
chr11:82404963..82428748hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3823786
hg1923786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459849
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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