A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459298



Internal ID21116851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47589401..47591300hg38UCSC Ensembl
chr11:47610953..47612852hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193790
Samples
Known GenesC1QTNF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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