A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451155



Internal ID21108708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27232400..27233449hg38UCSC Ensembl
chr11:27253947..27254996hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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