A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448396



Internal ID21105949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:277180..290570hg38UCSC Ensembl
chr11:277180..290570hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813391
hg1913391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185828
Samples
Known GenesATHL1, NLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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