A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467809



Internal ID21125362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123853392..123864769hg38UCSC Ensembl
chr11:123724100..123735477hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3811378
hg1911378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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