A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647832



Internal ID21596137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26669160..26669160hg38UCSC Ensembl
chr11:26690707..26690707hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074346
SamplesHG00732
Known GenesSLC5A12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647832
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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