A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455885



Internal ID21113438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124249621..124259343hg38UCSC Ensembl
chr11:124120368..124129239hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg389723
hg198872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181635
Samples
Known GenesOR8G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455885
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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