A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441172



Internal ID21098725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25920083..26008701hg38UCSC Ensembl
chr11:25941630..26030248hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3888619
hg1988619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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