A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442745



Internal ID21100298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:699104..843498hg38UCSC Ensembl
chr11:699104..843498hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38144395
hg19144395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195144
Samples
Known GenesCD151, CEND1, EFCAB4A, EPS8L2, NS3BP, PDDC1, PIDD, PNPLA2, POLR2L, RPLP2, SLC25A22, SNORA52, TALDO1, TMEM80, TSPAN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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