A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469462



Internal ID21127015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124463957..124464793hg38UCSC Ensembl
chr11:124333853..124334689hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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