A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469445



Internal ID21126998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128518701..128524200hg38UCSC Ensembl
chr11:128388596..128394095hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177238
Samples
Known GenesETS1, MIR6090
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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