A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472171



Internal ID21129724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134221901..134225500hg38UCSC Ensembl
chr11:134091795..134095394hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190131
Samples
Known GenesNCAPD3, VPS26B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472171
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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