A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466895



Internal ID21124448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32893401..32896800hg38UCSC Ensembl
chr11:32914947..32918346hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196119
Samples
Known GenesQSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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