A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469884



Internal ID21127437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128548201..128552400hg38UCSC Ensembl
chr11:128418096..128422295hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183088
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469884
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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