A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458832



Internal ID21116385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91599167..91608052hg38UCSC Ensembl
chr11:91332333..91341218hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg388886
hg198886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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