A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456107



Internal ID21113660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114378854..114380136hg38UCSC Ensembl
chr11:114249576..114250858hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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