A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455737



Internal ID21113290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100658416..100733365hg38UCSC Ensembl
chr11:100529147..100604096hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3874950
hg1974950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178482
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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