A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450668



Internal ID21108221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13158508..13160520hg38UCSC Ensembl
chr11:13180055..13182067hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382013
hg192013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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