A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450608



Internal ID21108161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16053401..16054600hg38UCSC Ensembl
chr11:16074947..16076146hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989438
Samples
Known GenesSOX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450608
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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