A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073752



Internal ID21409342
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 StatusS
Merged Variantsnsv5591666
Supporting Variants
SamplesHG00512
Known GenesSOX6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073752
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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