A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591666



Internal ID21540244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16201613..16201931hg38UCSC Ensembl
chr11:16223159..16223477hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073752
SamplesHG00512
Known GenesSOX6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591666
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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