A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436233



Internal ID21093786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28008317..28009124hg38UCSC Ensembl
chr11:28029864..28030671hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989851
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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