A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456741



Internal ID21114294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102303338..102315660hg38UCSC Ensembl
chr11:102174069..102186391hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3812323
hg1912323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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