A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454303



Internal ID21111856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22894265..22895043hg38UCSC Ensembl
chr11:22915811..22916589hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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