A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456676



Internal ID21114229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43321201..43322300hg38UCSC Ensembl
chr11:43342751..43343850hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991344
Samples
Known GenesAPI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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