A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451445



Internal ID21108998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22031339..22561000hg38UCSC Ensembl
chr11:22052885..22582546hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38529662
hg19529662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186321
Samples
Known GenesANO5, SLC17A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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