A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439467



Internal ID21097020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10395548..10407423hg38UCSC Ensembl
chr11:10417095..10428970hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811876
hg1911876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193274
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439467
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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