A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460377



Internal ID21117930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99746178..100811772hg38UCSC Ensembl
chr11:99616909..100682503hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381065595
hg191065595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192254
Samples
Known GenesARHGAP42, CNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460377
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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