A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468089



Internal ID21125642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91034181..91319164hg38UCSC Ensembl
chr11:90767349..91052331hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38284984
hg19284983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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