A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436754



Internal ID21094307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18504030..18505074hg38UCSC Ensembl
chr11:18525577..18526621hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188124
Samples
Known GenesTSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436754
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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