A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447565



Internal ID21105118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27456580..27465955hg38UCSC Ensembl
chr11:27478127..27487502hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg389376
hg199376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193861
Samples
Known GenesLGR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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