A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469778



Internal ID21127331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118990741..118996703hg38UCSC Ensembl
chr11:118861451..118867413hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385963
hg195963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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