A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463077



Internal ID21120630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114784872..114788296hg38UCSC Ensembl
chr11:114655594..114659018hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383425
hg193425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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