A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456095



Internal ID21113648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73469801..73503700hg38UCSC Ensembl
chr11:73180846..73214745hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3833900
hg1933900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193678
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456095
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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